NZ197854A - 5-substituted oxazolidine-2,4-diones and pharmaceutical compositions - Google Patents
5-substituted oxazolidine-2,4-diones and pharmaceutical compositionsInfo
- Publication number
- NZ197854A NZ197854A NZ197854A NZ19785481A NZ197854A NZ 197854 A NZ197854 A NZ 197854A NZ 197854 A NZ197854 A NZ 197854A NZ 19785481 A NZ19785481 A NZ 19785481A NZ 197854 A NZ197854 A NZ 197854A
- Authority
- NZ
- New Zealand
- Prior art keywords
- thienyl
- hydrogen
- oxazolidine
- dione
- product
- Prior art date
Links
- -1 5-substituted oxazolidine-2,4-diones Chemical class 0.000 title description 51
- 239000008194 pharmaceutical composition Substances 0.000 title description 3
- 239000000047 product Substances 0.000 claims description 235
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 228
- 239000011541 reaction mixture Substances 0.000 claims description 127
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 117
- 238000000034 method Methods 0.000 claims description 117
- 239000000203 mixture Substances 0.000 claims description 94
- 238000002360 preparation method Methods 0.000 claims description 86
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 84
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 81
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 80
- 150000001875 compounds Chemical class 0.000 claims description 66
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 65
- 239000001257 hydrogen Substances 0.000 claims description 45
- 229910052739 hydrogen Inorganic materials 0.000 claims description 45
- 238000001914 filtration Methods 0.000 claims description 36
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 28
- 239000002253 acid Substances 0.000 claims description 28
- 238000003756 stirring Methods 0.000 claims description 24
- 239000008280 blood Substances 0.000 claims description 19
- 210000004369 blood Anatomy 0.000 claims description 19
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 17
- 239000008103 glucose Substances 0.000 claims description 17
- 125000005843 halogen group Chemical group 0.000 claims description 17
- 239000000706 filtrate Substances 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 239000001301 oxygen Chemical group 0.000 claims description 8
- 229910052760 oxygen Chemical group 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 4
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 239000005909 Kieselgur Substances 0.000 claims description 3
- 230000003345 hyperglycaemic effect Effects 0.000 claims description 3
- RKEYPPBAGRFMSE-UHFFFAOYSA-N 4-methoxy-2-methylthiophene-3-carbaldehyde Chemical compound COC1=CSC(C)=C1C=O RKEYPPBAGRFMSE-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 2
- AGFXCIHFHWKQPQ-UHFFFAOYSA-N (4-methoxy-2-methylthiophen-3-yl)methanol Chemical compound COC1=CSC(C)=C1CO AGFXCIHFHWKQPQ-UHFFFAOYSA-N 0.000 claims 1
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 395
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 243
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 153
- 239000003921 oil Substances 0.000 description 141
- 235000019198 oils Nutrition 0.000 description 141
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 136
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 135
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 123
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 113
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 76
- COWNFYYYZFRNOY-UHFFFAOYSA-N oxazolidinedione Chemical compound O=C1COC(=O)N1 COWNFYYYZFRNOY-UHFFFAOYSA-N 0.000 description 75
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 60
- 239000007787 solid Substances 0.000 description 52
- 239000000243 solution Substances 0.000 description 49
- 239000012267 brine Substances 0.000 description 44
- 238000006243 chemical reaction Methods 0.000 description 44
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 44
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 44
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 43
- 229960000583 acetic acid Drugs 0.000 description 42
- 239000000284 extract Substances 0.000 description 38
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 29
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 28
- 239000010410 layer Substances 0.000 description 28
- HIMXGTXNXJYFGB-UHFFFAOYSA-N alloxan Chemical compound O=C1NC(=O)C(=O)C(=O)N1 HIMXGTXNXJYFGB-UHFFFAOYSA-N 0.000 description 26
- 239000000741 silica gel Substances 0.000 description 25
- 229910002027 silica gel Inorganic materials 0.000 description 25
- 238000001953 recrystallisation Methods 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 238000004458 analytical method Methods 0.000 description 22
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 22
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 22
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 22
- 238000001704 evaporation Methods 0.000 description 21
- 238000010992 reflux Methods 0.000 description 21
- 150000001299 aldehydes Chemical class 0.000 description 20
- 239000012043 crude product Substances 0.000 description 20
- 229940086542 triethylamine Drugs 0.000 description 20
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 19
- 150000002148 esters Chemical class 0.000 description 19
- 230000008020 evaporation Effects 0.000 description 19
- 229920006395 saturated elastomer Polymers 0.000 description 19
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 19
- 150000001477 2,4-oxazolidinediones Chemical class 0.000 description 18
- 239000012044 organic layer Substances 0.000 description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 17
- 230000002218 hypoglycaemic effect Effects 0.000 description 16
- 238000012544 monitoring process Methods 0.000 description 16
- 238000001665 trituration Methods 0.000 description 16
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 14
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical class [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 13
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 12
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 12
- 239000000543 intermediate Substances 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 11
- 239000008346 aqueous phase Substances 0.000 description 11
- 239000002585 base Substances 0.000 description 11
- 238000001816 cooling Methods 0.000 description 11
- 239000005457 ice water Substances 0.000 description 11
- 239000002243 precursor Substances 0.000 description 11
- ZIIHZVKHFWOENY-UHFFFAOYSA-N 5,5-dihydroxy-1,3-diazinane-2,4,6-trione Chemical compound OC1(O)C(=O)NC(=O)NC1=O ZIIHZVKHFWOENY-UHFFFAOYSA-N 0.000 description 10
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 10
- 239000002024 ethyl acetate extract Substances 0.000 description 10
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 9
- YNPAMTVSUKRXBH-UHFFFAOYSA-N 5-thiophen-3-yl-1,3-oxazolidine-2,4-dione Chemical compound O1C(=O)NC(=O)C1C1=CSC=C1 YNPAMTVSUKRXBH-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 150000002463 imidates Chemical class 0.000 description 9
- 239000012074 organic phase Substances 0.000 description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 8
- 239000000908 ammonium hydroxide Substances 0.000 description 8
- 239000003472 antidiabetic agent Substances 0.000 description 8
- 238000002425 crystallisation Methods 0.000 description 8
- 230000008025 crystallization Effects 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 150000002825 nitriles Chemical class 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 8
- 230000035484 reaction time Effects 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 8
- RBIGKSZIQCTIJF-UHFFFAOYSA-N 3-formylthiophene Chemical compound O=CC=1C=CSC=1 RBIGKSZIQCTIJF-UHFFFAOYSA-N 0.000 description 7
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 7
- 239000002775 capsule Substances 0.000 description 7
- 235000013877 carbamide Nutrition 0.000 description 7
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 239000012259 ether extract Substances 0.000 description 7
- 229940126904 hypoglycaemic agent Drugs 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 235000017557 sodium bicarbonate Nutrition 0.000 description 7
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 6
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 239000004202 carbamide Substances 0.000 description 6
- 238000004587 chromatography analysis Methods 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 238000002955 isolation Methods 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 239000012264 purified product Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 125000001544 thienyl group Chemical group 0.000 description 6
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 102000004877 Insulin Human genes 0.000 description 5
- 108090001061 Insulin Proteins 0.000 description 5
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 5
- 229940125396 insulin Drugs 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 150000003335 secondary amines Chemical group 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000006286 aqueous extract Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000002026 chloroform extract Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- CNUDBTRUORMMPA-UHFFFAOYSA-N formylthiophene Chemical compound O=CC1=CC=CS1 CNUDBTRUORMMPA-UHFFFAOYSA-N 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 239000012442 inert solvent Substances 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000020477 pH reduction Effects 0.000 description 4
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 4
- 239000001632 sodium acetate Substances 0.000 description 4
- 235000017281 sodium acetate Nutrition 0.000 description 4
- NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical compound O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 150000003512 tertiary amines Chemical class 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 238000010792 warming Methods 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
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- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
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- FSBVERYRVPGNGG-UHFFFAOYSA-N dimagnesium dioxido-bis[[oxido(oxo)silyl]oxy]silane hydrate Chemical compound O.[Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O FSBVERYRVPGNGG-UHFFFAOYSA-N 0.000 description 1
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- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- PSLIMVZEAPALCD-UHFFFAOYSA-N ethanol;ethoxyethane Chemical compound CCO.CCOCC PSLIMVZEAPALCD-UHFFFAOYSA-N 0.000 description 1
- WCHFOOKTKZYYAE-UHFFFAOYSA-N ethoxyperoxyethane Chemical compound CCOOOCC WCHFOOKTKZYYAE-UHFFFAOYSA-N 0.000 description 1
- XCRUQTHNHVXPMW-UHFFFAOYSA-N ethyl 2,4-dioxo-5-thiophen-3-yl-1,3-oxazolidine-3-carboxylate Chemical compound O=C1N(C(=O)OCC)C(=O)OC1C1=CSC=C1 XCRUQTHNHVXPMW-UHFFFAOYSA-N 0.000 description 1
- ORXTZQNYHALHPI-UHFFFAOYSA-N ethyl 2-(1-benzothiophen-3-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.C1=CC=C2C(C(O)C(=N)OCC)=CSC2=C1 ORXTZQNYHALHPI-UHFFFAOYSA-N 0.000 description 1
- RTBYBEHVDMVPAV-UHFFFAOYSA-N ethyl 2-(2-bromo-3h-thiophen-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1(Br)CC=CS1 RTBYBEHVDMVPAV-UHFFFAOYSA-N 0.000 description 1
- CROKJOHXTZFUMG-UHFFFAOYSA-N ethyl 2-(3-bromothiophen-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C=1SC=CC=1Br CROKJOHXTZFUMG-UHFFFAOYSA-N 0.000 description 1
- CZXAMLMPJNCSSD-UHFFFAOYSA-N ethyl 2-(4-bromothiophen-3-yl)-2-hydroxyethanimidate Chemical compound CCOC(=N)C(O)C1=CSC=C1Br CZXAMLMPJNCSSD-UHFFFAOYSA-N 0.000 description 1
- LZTIGJQHCXAILC-UHFFFAOYSA-N ethyl 2-(4-fluorothiophen-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC(F)=CS1 LZTIGJQHCXAILC-UHFFFAOYSA-N 0.000 description 1
- RXNUZGWLVQRTJR-UHFFFAOYSA-N ethyl 2-(4-fluorothiophen-3-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CSC=C1F RXNUZGWLVQRTJR-UHFFFAOYSA-N 0.000 description 1
- GLHMEJYWJAYKLV-UHFFFAOYSA-N ethyl 2-(5-bromofuran-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC=C(Br)O1 GLHMEJYWJAYKLV-UHFFFAOYSA-N 0.000 description 1
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- FYANPEDYMLXUGP-UHFFFAOYSA-N ethyl 2-(5-chlorofuran-2-yl)-2-hydroxyethanimidate Chemical compound CCOC(=N)C(O)C1=CC=C(Cl)O1 FYANPEDYMLXUGP-UHFFFAOYSA-N 0.000 description 1
- NGBQOSWQNXVICY-UHFFFAOYSA-N ethyl 2-(5-chlorofuran-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC=C(Cl)O1 NGBQOSWQNXVICY-UHFFFAOYSA-N 0.000 description 1
- IKQIGFDNIXFORQ-UHFFFAOYSA-N ethyl 2-(5-chlorothiophen-2-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC=C(Cl)S1 IKQIGFDNIXFORQ-UHFFFAOYSA-N 0.000 description 1
- VMEOVLDWYPGHAU-UHFFFAOYSA-N ethyl 2-(5-fluorothiophen-3-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CSC(F)=C1 VMEOVLDWYPGHAU-UHFFFAOYSA-N 0.000 description 1
- XQLUQRNGMFCKBR-UHFFFAOYSA-N ethyl 2-(6-fluoroquinolin-8-yl)-2-hydroxyacetate Chemical compound C1=CN=C2C(C(O)C(=O)OCC)=CC(F)=CC2=C1 XQLUQRNGMFCKBR-UHFFFAOYSA-N 0.000 description 1
- VGPSLUDWDOOSBG-UHFFFAOYSA-N ethyl 2-(6-fluoroquinolin-8-yl)-2-hydroxyacetate 2-(6-fluoroquinolin-8-yl)-2-hydroxyacetamide Chemical compound FC=1C=C2C=CC=NC2=C(C1)C(C(=O)OCC)O.FC=1C=C2C=CC=NC2=C(C1)C(C(=O)N)O VGPSLUDWDOOSBG-UHFFFAOYSA-N 0.000 description 1
- SIDUNVQRCQLIRQ-UHFFFAOYSA-N ethyl 2-(6-fluoroquinolin-8-yl)-2-oxoacetate Chemical compound C1=CN=C2C(C(=O)C(=O)OCC)=CC(F)=CC2=C1 SIDUNVQRCQLIRQ-UHFFFAOYSA-N 0.000 description 1
- XSJFFMSYTTXAIC-UHFFFAOYSA-N ethyl 2-(furan-3-yl)-2-hydroxyethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C=1C=COC=1 XSJFFMSYTTXAIC-UHFFFAOYSA-N 0.000 description 1
- ICFGZPRDSWOEAD-UHFFFAOYSA-N ethyl 2-hydroxy-2-(1,2-thiazol-5-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC=NS1 ICFGZPRDSWOEAD-UHFFFAOYSA-N 0.000 description 1
- OCLMXKKTOPRMTB-UHFFFAOYSA-N ethyl 2-hydroxy-2-(3-methyl-1,2-oxazol-5-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC(C)=NO1 OCLMXKKTOPRMTB-UHFFFAOYSA-N 0.000 description 1
- AOVPZKNKWJTUBJ-UHFFFAOYSA-N ethyl 2-hydroxy-2-(4-methoxy-2-methylthiophen-3-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=C(C)SC=C1OC AOVPZKNKWJTUBJ-UHFFFAOYSA-N 0.000 description 1
- SQCXUBAVFABACS-UHFFFAOYSA-N ethyl 2-hydroxy-2-(4-methoxythiophen-3-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CSC=C1OC SQCXUBAVFABACS-UHFFFAOYSA-N 0.000 description 1
- DHDDOGJMCRWHEA-UHFFFAOYSA-N ethyl 2-hydroxy-2-(4-propoxythiophen-3-yl)ethanimidate;hydrochloride Chemical compound Cl.CCCOC1=CSC=C1C(O)C(=N)OCC DHDDOGJMCRWHEA-UHFFFAOYSA-N 0.000 description 1
- WCYNPFPLQUSFEG-UHFFFAOYSA-N ethyl 2-hydroxy-2-(5-methyl-1,2-oxazol-3-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C=1C=C(C)ON=1 WCYNPFPLQUSFEG-UHFFFAOYSA-N 0.000 description 1
- OLLBLDQUMYZNLM-UHFFFAOYSA-N ethyl 2-hydroxy-2-(5-methylfuran-2-yl)ethanimidate;hydrochloride Chemical compound Cl.CCOC(=N)C(O)C1=CC=C(C)O1 OLLBLDQUMYZNLM-UHFFFAOYSA-N 0.000 description 1
- VETSRFBHLSETOJ-UHFFFAOYSA-N ethyl 2-hydroxy-2-thiophen-2-ylethanimidate 2-thiophen-2-yl-2-trimethylsilyloxyacetonitrile Chemical compound S1C(=CC=C1)C(C#N)O[Si](C)(C)C.OC(C(OCC)=N)C=1SC=CC1 VETSRFBHLSETOJ-UHFFFAOYSA-N 0.000 description 1
- UVJRKQMWSKOSOF-UHFFFAOYSA-N ethyl 2-hydroxy-2-thiophen-3-ylacetate Chemical compound CCOC(=O)C(O)C=1C=CSC=1 UVJRKQMWSKOSOF-UHFFFAOYSA-N 0.000 description 1
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- FKRDHSJRDDPBEL-UHFFFAOYSA-N ethyl 4-ethoxythiophene-3-carboxylate Chemical compound CCOC(=O)C1=CSC=C1OCC FKRDHSJRDDPBEL-UHFFFAOYSA-N 0.000 description 1
- KNDWQLSUXRVOQN-UHFFFAOYSA-N ethyl 4-hydroxy-2-methylthiophene-3-carboxylate ethyl 4-methoxy-2-methylthiophene-3-carboxylate Chemical compound OC=1C(=C(SC1)C)C(=O)OCC.COC=1C(=C(SC1)C)C(=O)OCC KNDWQLSUXRVOQN-UHFFFAOYSA-N 0.000 description 1
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- 239000013505 freshwater Substances 0.000 description 1
- WGDBHJNTIVIRRV-UHFFFAOYSA-N furan-2-carbaldehyde 2-(furan-2-yl)-1,3-dioxolane Chemical compound O1C(=CC=C1)C=O.O1C(=CC=C1)C1OCCO1 WGDBHJNTIVIRRV-UHFFFAOYSA-N 0.000 description 1
- BTUIFMCWPFMNRG-UHFFFAOYSA-N furan-3-carbonyl chloride Chemical compound ClC(=O)C=1C=COC=1 BTUIFMCWPFMNRG-UHFFFAOYSA-N 0.000 description 1
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- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 1
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- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- OLNJUISKUQQNIM-UHFFFAOYSA-N indole-3-carbaldehyde Chemical class C1=CC=C2C(C=O)=CNC2=C1 OLNJUISKUQQNIM-UHFFFAOYSA-N 0.000 description 1
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- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
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- 230000007794 irritation Effects 0.000 description 1
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- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- QUFUZPOMGMZNNL-UHFFFAOYSA-N lithium;2h-1,3-thiazol-2-ide Chemical compound [Li+].C1=CS[C-]=N1 QUFUZPOMGMZNNL-UHFFFAOYSA-N 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- AXLHVTKGDPVANO-UHFFFAOYSA-N methyl 2-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate Chemical compound COC(=O)C(N)CNC(=O)OC(C)(C)C AXLHVTKGDPVANO-UHFFFAOYSA-N 0.000 description 1
- LYDBGZWFDPWYOF-UHFFFAOYSA-N methyl 4-hydroxythiophene-3-carboxylate Chemical compound COC(=O)C1=CSC=C1O LYDBGZWFDPWYOF-UHFFFAOYSA-N 0.000 description 1
- XEXPJABJVHEOCX-UHFFFAOYSA-N methyl 4-methylpyridine-3-carboxylate Chemical compound COC(=O)C1=CN=CC=C1C XEXPJABJVHEOCX-UHFFFAOYSA-N 0.000 description 1
- KHGQMIBDLPEOCL-UHFFFAOYSA-N methyl 5-chloro-2-methoxypyridine-3-carboxylate Chemical compound COC(=O)C1=CC(Cl)=CN=C1OC KHGQMIBDLPEOCL-UHFFFAOYSA-N 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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- 229940127209 oral hypoglycaemic agent Drugs 0.000 description 1
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- 125000001979 organolithium group Chemical group 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
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- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
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- ICFJFFQQTFMIBG-UHFFFAOYSA-N phenformin Chemical compound NC(=N)NC(=N)NCCC1=CC=CC=C1 ICFJFFQQTFMIBG-UHFFFAOYSA-N 0.000 description 1
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- 229940093932 potassium hydroxide Drugs 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- WVQCDOLBWQGTMX-UHFFFAOYSA-N potassium;1h-pyrrole Chemical compound [K].C=1C=CNC=1 WVQCDOLBWQGTMX-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- ZMRUPTIKESYGQW-UHFFFAOYSA-N propranolol hydrochloride Chemical compound [H+].[Cl-].C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 ZMRUPTIKESYGQW-UHFFFAOYSA-N 0.000 description 1
- MGESDDNXOPAKNI-UHFFFAOYSA-N propyl 4-propoxythiophene-3-carboxylate Chemical compound CCCOC(=O)C1=CSC=C1OCCC MGESDDNXOPAKNI-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- HREHOXSRYOZKNT-UHFFFAOYSA-N quinolin-2-ylmethanol Chemical compound C1=CC=CC2=NC(CO)=CC=C21 HREHOXSRYOZKNT-UHFFFAOYSA-N 0.000 description 1
- OVYWMEWYEJLIER-UHFFFAOYSA-N quinolin-6-ol Chemical compound N1=CC=CC2=CC(O)=CC=C21 OVYWMEWYEJLIER-UHFFFAOYSA-N 0.000 description 1
- XCRPPAPDRUBKRJ-UHFFFAOYSA-N quinolin-7-ol Chemical compound C1=CC=NC2=CC(O)=CC=C21 XCRPPAPDRUBKRJ-UHFFFAOYSA-N 0.000 description 1
- OVZQVGZERAFSPI-UHFFFAOYSA-N quinoline-8-carbaldehyde Chemical compound C1=CN=C2C(C=O)=CC=CC2=C1 OVZQVGZERAFSPI-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 238000010956 selective crystallization Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- BFVCNOLEHBUKQW-UHFFFAOYSA-N sodium;5-thiophen-3-yl-1,3-oxazolidine-2,4-dione Chemical compound [Na].O1C(=O)NC(=O)C1C1=CSC=C1.O1C(=O)NC(=O)C1C1=CSC=C1 BFVCNOLEHBUKQW-UHFFFAOYSA-N 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000008227 sterile water for injection Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 229960002277 tolazamide Drugs 0.000 description 1
- OUDSBRTVNLOZBN-UHFFFAOYSA-N tolazamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)NN1CCCCCC1 OUDSBRTVNLOZBN-UHFFFAOYSA-N 0.000 description 1
- 229960005371 tolbutamide Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 229940124586 β-lactam antibiotics Drugs 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/513—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an etherified hydroxyl group
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/18—Halogen atoms or nitro radicals
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
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- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/28—Halogen atoms
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
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- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
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Description
New Zealand Paient Spedficaiion for Paient Number 1 97854
1 97
j Prioritv .7
J ' 1 <27- 7 - 0 /
L a m ■ i'o ^ <«' 1 k f\t I A /■ a1> 0*1 f er' f*/IT"7 C / o
JQ, ■ ■ a ■
1984
P^it-
U/j feiii k itij&d ^
No.:
NEW ZEALAND, PATENTS ACT, 1953
•vM
Date:
COMPLETE SPECIFICATION
"HYPOGLYCEMIC 5-SUBSTITUTED 0XAZ0LIDINE-2,4-DIONES"
k^We- PFIZER INC,, a corporation organized under the laws of the State of Delaware, United States of America, of 235 East 42nd Street, New York, State of New York, United States of America,
hereby declare the invention for which £ / we pray that a patent may be granted to me^us, and the method by which it is to be performed, to be particularly described in and by the following statement:-
- 1 - (followed by page la)
* • 197
O 3
P.C. (Ph) 02GOD/C
"1<X~
HYPOGLYCEMIC 5-SUBSTITUTED OXAZOLlDINE-2,4-DIONES The present invention relates to certain 5-furyl, 5-thienyl, 5-chromanyl, 2,3-dihydrobenzo[b]furanyl, 5-pyridyl, 5-quinolyl, 5-pyrrolyl, 5-indolyl, 5-5 thiazolyl, 5-oxazolyl, 5-isothiazolyl and 5-isoxazolyl derivatives of oxazolidine-2,4-dione having utility as hypoglycemic agents.
In spite of the early discovery of insulin and its subsequent wide-spread use in the treatment of 10 diabetes, and the later discovery and use of sulfonylureas (e.g., chlorpropamide, tolbutamide, acetohexamide, tolazamide) and biguanides (e.g., phenformin) as oral hypoglycemic agents, the treatment of diabetes remains less than satisfactory. The use of insulin, necessary 15 in a high percentage of diabetics where available synthetic hypoglycemic agents are not effective,
requires multiple daily, usually self, injection. Determination of the proper dosage of insulin requires frequent estimations of the sugar in the urine or in 20 the blood. The administration of an excess dose of insulin causes hypoglycemia, with effects ranging from mild abnormalities in blood glucose to coma, or even death. Where effective, a synthetic hypoglycemic agent is preferred over insulin, being more convenient 25 to administer and less prone to cause severe hypoglycemic reactions. However, the clinically available hypoglycemics are unfortunately fraught with other toxic manifestations which limit their use. In any event, where one of these agents may fail in an 30 individual case, another may succeed. A continuing need for hypoglycemic agents, which may be less toxic or succeed where others fail, is clearly evident.
In addition to the hypoglycemic agents cited above, a variety of other compounds have been reported 35 to possess this type of activity, as reviewed recently
1 97
by Blank [Burger's Medicinal Chemistry, Fourth Edition Part II, John Wiley and Sons, N.Y. (1979), pp. 1057-1080].
The oxazolidine-2,4-diones of the present in-5 vention are novel compounds; this in spite of the fact that the oxazolidine-2,4-diones are broadly known as a class of compounds [for an extensive review, see Clark-Lewis, Chem. Rev. 58, pp. 63-99 (1958)]. Among the compounds known in this class are 10 5-phenyloxazolidine-2,4-dione, variously reported as an intermediate to certain beta-lactam antibacterial agents (Sheehan, U.S. Patent 2,721,197), as an antidepressant agent (Plotnikoff, U.S. Patent 3,699,229) and as an anticonvulsant agent [Brink and Freeman, J. 15 Neuro. Chem. 19 (7), pp. 1783-1788 (1972)]; a number of 5-phenyloxazolidine-2,4-diones substituted on the phenyl ring, e.g., 5-(4-methoxyphenyl)oxazolidine-2,4-dione [King and Clark-Lewis, J. Chem. Soc. , pp. 3077-3079 (1961)], 5-(4-chlorophenyl)oxazolidine-2,4-20 dione [Najer et al. , Bull. soc. chim. France, pp.
1226-1230 (1961)], 5-(4-methylphenyl)oxazolidine-2,4-dione [Reibsomer ^t al., J. Am. Chem. Soc. 61, pp. 3491-3493 (1939)], and 5-(4-aminophenyl)oxazolidine-2,4-dione (German Patent 108,026); and 5-(2-pyrryl)-25 oxazolidine-2,4-dione [Ciamacian and Silber, Gazz. chim. ital. 16, 357 (1886); Ber. 19, 1708-1714 (1886)]. The last-named compound, having no prior known utility, shows only relatively weak hypoglycemic activity (vide post. Table I). 30 Oxazolidine-2,4-dione and substituted oxazolidine
2,4-diones (specifically, the 5-methyl and 5,5-dimethyl derivatives) have been reported as acid moieties suitable for forming acid-addition salts with the hypoglycemic, basic biguanides (Shapiro and 35 Freedman, U.S. Patent 2,961,377). We have determined
• 1 97
that neither oxazolidine-2,4-dione itself, nor 5,5-dimethyloxazolidine-2,4-dione possess the hypoglycemic activity of the compounds of the present invention.
Recently, a group of spiro-oxazolidine-2,4-dione 5 derivatives have been reported which are aldose reductase inhibitors, thus finding utility in the treatment of certain complications of diabetes (Schnur, U.S. Patent 4,200,642).
A process for the synthesis of 3-aryloxazolidine-10 2,4-diones (wherein said aryl group is 6 to 12 carbon atoms, unsubstituted or substituted with one or more halogen atoms, methyl or methoxy) is the subject of another recent U.S. Patent (Scholz, U.S. 4,220,787). The utility of these compounds is not specified. 15 The present invention is concerned with compounds of the formula
0
(1)
wherein
R is hydrogen, (C^-C4)-alkanoyl (e.g., formyl, acetyl, isobutyryl), benzoyl, (C2~C4)-carbalkoxy (e.g., carbomethoxy, carbethoxy, carboisopropoxy), (C^-C^)-alkylcarbamoyl (e.g., N-methylcarbamoyl, N-propylcarbamoyl), (C^-C^)-cycloalkylcarbamoyl (e.g., N-cyclohexylcarbamoyl) or di-(C^-C^)-dialkylcarbamoyl 25 (e.g., N,N-dimethylcarbamoyl); and R^" is:
#
.1 97
(a)
or
R'
R"
wherein R1 is (C^-C^Jalkyl or phenyl, R" is hydrogen, (Cj-C4)alkyl or phenyl and X is halo (fluoro, chloro, 5 bromo or iodo); these formulae are intended to encompass 2- or 3-pyrrolyl and indolyl derivatives, with substituents as specified;
wherein Y is hydrogen or (C^-C3)alkoxy, Y' is hydrogen 10 or (C^-C^alkyl and Y" is hydrogen or halo;
wherein Z' is hydrogen, halo or (C^-C^Jalkoxy and Z" is hydrogen or halo;
(b)
(c)
or
(d)
wherein W is hydrogen or halo, and n is 1 or 2; these formula are intended to encompass 6- or 7-halo-8-chromanyl or 5- or 6-halo-7-benzofuranyl derivatives;
(e)
or wherein Q is sulfur or oxygen and V is hydrogen or (C1~C3)alkyl; or
(f)
wherein Q is sulfur or oxygen; and V is hydrogen or (C^-C^Jalkyl; these formula are intended to encompass 3-, 4- and 5-isothiazolyl and isoxazolyl derivatives;
(
(9)
:SrJ3r or wherein Y is sulfur or oxygen; X is hydrogen, fluoro,
chloro, bromo, iodo, methyl, phenyl, benzoyl or (C.-C^)
1 2
alkoxy; X is hydrogen or methyl; and X is hydrogen,
fluoro, chloro, bromo or iodo; when X* is hydrogen,
the first formula is intended to encompass the full gamut of 5-(2-furyl)-, 5-(3-furyl)-, 5-(2-thienyl)-
and 5-(3-thienyl)-derivatives of oxazolidine-2,4-
dione wherein the substituent X can be attached to
any vacant carbon position of the furan/thiophene ring, i.e.,
4
tx x
where X and Y are as defined above and Ox is used as an abbreviation for the oxazolidin-2,4-dione ring attached at the 5-position; when both X and X^" are other than hydrogen, the second substituent can be inserted at either vacant position in any one of these six variants; the second formula is intended to encompass those compounds wherein the oxazolidine is substituted at the 2-, 3- or 7-position of the benzo[b]furan/benzo[b]thiophene ring system, i.e.
*
1
Ox
The invention also encompasses the pharmaceutically acceptable cationic salts of compounds of the formula (1) when R is hydrogen, as well as the pharmaceutically acceptable acid addition salts thereof when R"*"
contains a basic nitrogen function.
It is believed that the inherent, high activity of these compounds resides primarily in those compounds wherein R is hydrogen, and that those compounds wherein R is one of a variety of carbonyl derivatives defined above represent so-called pro-drugs, i.e., the carbonyl side chain is removed by hydrolysis under physiological conditions, yielding the fully-active compounds wherein R is hydrogen.
The expression "pharmaceutically acceptable cationic salts" is intended to define such salts as the alkali metal salts, (e.g., sodium and potassium), alkaline earth metal salts (e.g., calcium and magnesium), aluminum salts, ammonium salts, and salts with organic amines such as benzathine (N,N*-dibenzylethylenediamine), choline, diethanolamine, ethylenediamine, meglumine (N-methylglucamine), benethamine (N-benzylphenethylamine), diethylamine, piperazine, tromethamine (2-amino-2-hydroxymethyl-1,3-propanediol), procaine, etc.
The expression "pharmaceutically acceptable acid addition salts" is intended to include such salts as the hydrochloride, hydrobromide, hydroiodide, nitrate, hydrogen sulfate, dihydrogen phosphate, mesylate,
maleate, succinate, etc.
The compounds of the present invention possess hypoglycemic activity, reflecting their clinical utility in the lowering of the blood glucose level of hyperglycemic mammals, including man, to normal values. They have the special advantage of lowering
I 97
* ff O
blood glucose values to a normal range without danger of causing hypoglycemia. The compounds of the present invention are tested for hypoglycemic (anti-hyper-glycemic) activity in rats, using the so-called 5 glucose tolerance test, as described in greater detail hereinafter.
Preferred compounds, because of their better hypoglycemic activity, are those wherein R is hydrogen, or the pharmaceutically acceptable salts thereof.
Among those compounds of the formula (1) wherein R is hydrogen, the most preferred compounds, because of their excellent hypoglycemic activity, are:
-(l-methyl-2-pyrrolyl)oxazolidine-2,4-dione; 5-(l-ethyl-2-pyrrolyl)oxazolidine-2,4-dione;
5-(l-phenyl-2-pyrrolyl)oxazolidine-2,4-dione;
-(2-methoxy-3-pyridyl)oxazolidine-2,4-dione; 5-(2-ethoxy-3-pyridyl)oxazolidine-2,4-dione; 5-(5-chloro-2-methoxy-3-pyridyl)oxazolidine-2,4-dione;
5-(5-chloro-2-ethoxy-3-pyridyl)oxazolidine-2,4-
dione;
-(8-quinolyl)oxazolidine-2,4-dione;
-(7-methoxy-8-quinolyl)oxazolidine-2,4-dione;
-(6-chloro-8-quinolyl)oxazolidine-2,4-dione;
5-(6-fluoro-8-quinolyl)oxazolidine-2,4-dione;
-(2-benzthiazolyl)oxazolidine-2,4-dione; 5-(2-thiazolyl)oxazolidine-2,4-dione; 5-(6-chloro-8-chromanyl)oxazolidine-2,4-dione; 5-(6-fluoro-8-chromanyl)oxazolidine-2,4-dione;
5-(5-chloro-2,3-dihydro-7-benzofuranyl)oxazolidine-
2,4-dione;
-(3-methyl-5-isoxazolyl)oxazolidine-2,4-dione; 5-(3-thienyl)oxazolidin-2,4-dione;
-(4-bromo-3-thienyl)oxazolidin-2,4-dione;
-(4-ethoxy-3-thienyl)oxazolidin-2,4-dione;
-(4-ethoxy-2-methyl-3-thienyl)oxazolidin-2,4-dione;
5-(4-methoxy-2-methyl-3-thienyl)oxazolidin-2,4-
dione;
-(3-methyl-2-thienyl)oxazolidin-2,4-dione;
-(3-methoxy-2-thienyl)oxazolidin-2,4-dione;
-(3-furyl)oxazolidin-2,4-dione; 10 5-(2-fury1)oxazolidin-2,4-dione;
-(3-bromo-2-fury1)oxazolidin-2,4-dione;
-(5-chloro-2-furyl)oxazolidin-2,4-dione;
-(7-benzo[b]thienyl)oxazolidin-2,4-dione; and
-(5-chloro-7-benzo[b]furanyl)oxazolidin-2,4-15 dione.
The compounds of the present invention are prepared by a variety of methods, as summarized in Flowsheet I, wherein
R^" is as defined above;
2
R is lower alkyl (e.g. methyl or ethyl);
3
R is hydrogen, lower alkyl or phenyl; and
4
R is hydrogen, or acyl such as acetyl or benzoyl.
A particularly convenient synthesis for compounds 25 of the present invention is via carboximidate (3). The latter compound is reacted with phosgene in an inert solvent such as tetrahydrofuran in the presence of 2 to 2.3 equivalents of a tertiary amine (e.g. triethylamine, N-methylmorpholine). A further equivalent 30 of tertiary amine is used if the carboximidate is introduced as the acid addition salt (e.g. hydrochloride salt). The temperature of the reaction is not critical, but lower temperatures (e.g. -10° to 10°C.) are preferred during the initial stages of the
Flowsheet I Oxazolidine-2,4-dione Precursors r4O ^-nh
reaction, particularly if it is desired to isolate the intermediate 4-alkoxyoxazol-2-one (4). Isolation of this intermediate is carried out by simple evaporation of the reaction mixture to dryness. On further reaction at higher temperatures (e.g. 20°-150°C.) or on aqueous work-up the intermediate (4) is converted to the desired oxazolidine-2,4-dione. When a primary or secondary amine function is desired in the final product, this functionality is introduced via an oxazolidine-2,4-dione containing a group selectively reducible (e.g. by catalytic hydrogenation or acid/ metal couple) to the primary or secondary amine. For example an N-benzylindole can be used as a precursor for an indole derivative.
Th e carboximidate (3) is conveniently prepared from the corresponding aldehyde by the sequence:
R1CHO (11)
(13)
The aldehyde (11) is converted to the cyanohydrin 5 (13) by standard procedures (e.g. via the bisulfite adduct, which is reacted with cyanide in a two phase, aqueous-organic solvent system). Alternatively, the aldehyde is converted to the trimethylsilyl cyanohydrin (12) by reaction with trimethylsilylcarbonitrile 10 in the presence of a catalytic quantity of a Lewis acid, e.g., zinc iodide. A reaction inert solvent (e.g. methylene chloride, ether) is generally used when the aldehyde is a solid, but is optional when the aldehyde is a liquid. The temperature of the 15 reaction is not critical, it being conveniently made up at reduced temperature (e.g. 0-5°C.) and allowed to proceed at room temperature for a matter of hours or days, as necessary to achieve complete reaction. If desired, the trimethylsilyl ether can be hydrolyzed 20 to cyanohydrin, conveniently at reduced temperature
(e.g. -10°C.) in a two phase strong aqueous acid/organic solvent system.
osi(CH3)3
Either the cyanohydrin (13) or the trimethylsilyl ether (12) is converted to the carboximidate (3) by strong acid catalyzed alcoholysis (using strictly anhydrous conditions). A convenient method is to 5 simply dissolve the nitrile in alcohol which has been saturated with hydrogen chloride) and allow the solution to stand until carboximidate formation is complete. Temperature is not critical, although lower temperatures (e.g. 0-25°C.) generally lead to 1° more optimal yields.
The aldehydes required for the above syntheses are broadly available either commercially, or by literature methods. For example, N-alkylpyrrole-2-carbaldehydes are obtained by alkylation of pyrrole-15 2-carbaldehyde (Weygand, Organic Preparations, Interscience, New York, 1945, p. 403) using conditions specifically exemplified hereinafter for the preparation of N-alkylpyrroles, or by Reimer-Tieman formylation of N-alkylpyrrole (£f Weygand loc. cit.); 3-formylindoles 20 are similarly obtained from indoles [cf_ Boyd and
Robson, Biochem J. 29, p. 555 (1935; Shabica et al., J. Am. Chem. Soc. 68, p. 1156 (1946)]; Rosenmund hydrogenation of the corresponding acid chloride [e.g. 3-furaldehyde; Hayes, J. Am. Chem. Soc. 71,
2581 (1949)], from halomethyl compounds by the Sommelet reaction [e.g. 3-thenaldehyde; Campaigne and LaSuer, J. Am. Chem. Soc. 70, 1557 (1948)], formylation [e.g. 2-thenaldehyde, 3-methyl-2-thenaldehyde, 5-methyl-2-thenaldehyde; Watson and Michaels, J. Am. Chem. Soc. 30 72, 1422 (1950), Organic Syntheses 31, 108 (1951); 3-bromo-2-thenaldehyde; Elliott et al., J. Chem. Soc. (C), 2551 (1971)]; reduction of chloromethyl substituted aldehydes [e.g. 5-methyl-2-furaldehyde, Spence and Wild, J. Chem. Soc., 338 (1935)], oxidation of the 35 corresponding alcohol [e.g. 2-thenaldehyde; Emerson
CO>*77 a CO)
and Patrick, J. Org. Chem., 14, 790 (1949)], interaction of Grignard reagents with orthoformic esters [e.g. 2-thenaldehdye; Cagniant, Bull. soc. chim. France 16, 849 (1949)], decarboxylation of alpha-keto acids 5 [e.g. 2-thenaldehyde; Barger and Easson, J. Chem.
Soc., 2100 (1938)], and halogenation [e.g. 2-bromo-3-thenaldehyde; Elliot et al., loc. cit.]; a variety of the presently required aldehydes are further available by the hydrolysis of gem-dihalides, oxidation of 10 primary alcohols, interaction of Grignard reagents with orthoformic esters and other methods known in the art. Additional methods are noted in the Preparations detailed hereinafter.
Another suitable precursor for those oxazolidine-15 2,4-diones of the present invention lacking a primary or secondary amine function is the alpha-hydroxy amide (5). The latter compound is converted to the desired oxazolidine-2,4-dione (1), either by reaction with alkyl chloroformate in the presence of a basic 20 catalyst such as potassium carbonate, or by reaction with a dialkyl carbonate in the presence of a more strongly basic catalyst such as sodium methoxide or potassium tert-butoxide. An alcohol is generally suitable as solvent for the latter reaction with 1 to 25 3 equivalents of both dialkyl carbonate and base
' employed, preferably 2-3 equivalents of each. When a primary or secondary amine function is desired in the final product, this functionality is introduced via an oxazolidine-2,4-dione containing a suitable precursor 30 group, as described above.
The required alpha-hydroxy amide is conveniently prepared from cyanohydrin (13) or from alpha-hydroxy acid or ester (6):
OH
0
R
1
CN
'R
2
(13)
\
1-
OH
H
2
(6)
R
O
Convenient conditions for the hydrolysis of the cyanohydrin (13) are to treat the cyanohydrin in formic acid with excess concentrated hydrochloric acid. A temperature range of 0-75°C. is generally satisfactory, depending upon the stability of the individual amide in this medium. If desired, an intermediate formate ester of (5) can be isolated under these conditions. Over hydrolysis to the acid can be avoided by tic monitoring of the reaction, as detailed below. Convenient conditions for the aminolysis of ester (6) are to simply heat the ester in hot concentrated ammonium hydroxide.
The alpha-hydroxy ester (6) itself can also be employed as the immediate precursor of the desired oxazolidine-2,4-dione. The ester is reacted with urea (or one of certain substituted ureas, such as phenyl urea or l-acetyl-3-methylurea) in the presence of a basic catalyst such as sodium ethoxide (suitably 1 equivalent) in alcohol at a temperature of 50-110°C. The ester to be used for this purpose is by no means restricted to a simple lower alkyl ester, but can be any one of a broad variety of esters, e.g. phenyl, benzyl, etc. Furthermore, the ester can be replaced by a 1,3-dioxolan-4-one, an alpha-acyloxy ester or a thioester e.g.,
V / o
CH CH-.
| J | *5
c=o c=o
1 I
0 or 0
R1'X^V|^OC2H5 R1^^/SCH3
0 0
and the urea can be replaced by a urethan.
Two other precursors suitable for the synthesis of the desired oxazolidine-2,4-diones are the thio 5 compounds (7) and (8). The 2-thioxo compound (7) is converted to the desired oxazolidine-2,4-diones under oxidative conditions, e.g. mercuric ion, aqueous bromine or chlorine, metaperiodate, or aqueous hydrogen peroxide, usually in excess and in the 10 presence of a co-solvent, such as a lower alcohol.
The temperature of reaction is not critical, temperatures in the range 25-100°C. being generally satisfactory. Other methods are usually preferred when R^" has an amine function, since competing oxidation at 15 the nitrogen tends to reduce yields and complicates isolation of the desired product; it has been found, however, that when the product contains a tert-amine (e.g., pyridine, quinoline), that periodate or bromine are reagents well-suited for this purpose. The 20 oxazolidine-2,4-diones are obtained from the alkyl-thio compounds (8) by simple acid or base catalyzed hydrolysis. Preferable conditions are aqueous hydrochloric acid in a temperature range of 0-50°C.
The precursor 2-thioxo compound (7) is prepared 25 from the corresponding aldehyde (11), generally accomplished in an aqueous acidic media by the action of thiocyanate (1-1.1 equivalents) and cyanide (1 to 1.2 equivalents) at 0-70°C., following the method of
1 9785
Lindberg and Pederson by which method the preparation of 5-(2-thienyl)-2-thiooxazolidin-4-one has been reported [Acta Pharm. Suecica 5 (1), pp. 15-22 (1968); Chem. Abstr. 69, 52050k], The precursor 2-alkylthio 5 compounds (8) can be prepared by alkylation of the 2-thioxo compounds (7), e.g. with an alkyl halide or dialkyl sulfate, preferably in the presence of at least two equivalents of a base such as a lower alkoxide in a reaction inert solvent such as a lower 10 alkanol. The 3-alkyl derivative can be a by-product of this reaction.
Also suitable as a precuror is the 2-imino-oxa-zolidine-4-one derivative (9), readily hydrolyzed to the oxazolidine-2,4-dione, preferably under aqueous 15 acid conditions. The required 2-iminooxazolidin-4-one is obtained by condensation of the alpha-hydroxy ester (6) with guanidine or with thiourea in the presence of one equivalent of a strong base such as sodium alkoxide, by ammonolysis of the 2-alkoxy 20 compound (isomeric with 4) or the 2-thioalkyl compound
(8), by alkali induced cyclization of the appropriate
1 3
alpha-halogenureides (R CHZCONHCONHR wherein Z is a halogen such as chloro or bromo), or by the condensation
1 2
of the appropriate alkyl alpha-haloacetates (R CHZCOOR ) 25 with urea or a substituted urea (R^NHCONH2).
Ammonolysis of the 4-alkoxy derivatives (4)
yields 4-imino derivatives (isomeric with 9). The latter compounds are also readily hydrolyzed to oxazolidine-2 , 4-diones. The 4-alkoxy derivatives them-30 selves are also prepared from the silver salt of the desired oxazolidine-2,4-dione.
Also highly useful as precursors of the oxazolidine-2 , 4-diones of the present invention are the dialuric acids and acyl dialuric acids (10). These
• l19 78
are readily converted, under mildly basic conditions, to the desired oxazolidine-2,4-diones. Methods suitable for the preparation of precursor dialuric acids
(10) are shown in Flowsheet II, wherein the substit-c 12 4
uents R , R and R are as defined above, and M is Li, MgCl, MgBr, Mgl, or other suitable metal.
A general method for preparing dialuric acids appropriate as precursors of the oxazolidine-2,4-diones of the present invention is from the malonic 10 ester derivatives (14), involving the two stages of base catalyzed condensation with urea and oxidation to the hydroxy or acyloxy compound. When the first stage is oxidation, the intermediate is a so-called tartronic acid derivative (15), while when the first 15 stage is condensation, the intermediate is a so-called barbituric acid (16). When R* contains an amine function (e.g. 2-aminophenyl), it is preferred to carry out oxidation as the first stage, preventing possible complications of nitrogen oxidation. When 20 condensation is the second stage, the dialuric acid is usually not isolated, at least in pure form, and is further converted, under basic conditions of the condensation, to the oxazolidine-2,4-dione.
Flowsheet II ■%> ■
(10)
°\>—NH
is>
(16)
COOR2
1' 4 R C-OR
1 2
COOR
(15)
COOR2 1 »
R CH
' 2
COOR
(14)
The substituted malonic esters required for the above syntheses, when not available commercially, are obtained by literature methods, such as alcoholysis of alpha-cyano esters [cf. Steele, J. Am. Chem. Soc. 53, 286 (1931)], carbalkoxylation of esters [cf. Horning and Finelli, Org. Syntheses 30, 43 (1950)] and decarbonylation of alpha-keto esters obtained by the condensation of dialkyl oxalate with carboxylate esters [Reichstein and Morsman, Helv. Chim. Acta 17, 1123 (1934); Blicke and Zienty, J. Am Chem. Soc. 63, 2946 (1941)].
A less general method for the preparation of the appropriate dialuric acid intermediate is to react an electron rich heteroaryl/aryl compound, e.g.,
X
* // \>
Now available is yet another method for the preparation of certain dialuric acid intermediates. This method, preferred when the appropriate starting materials are readily available, involves the reaction
of alloxan (preferably in anhydrous form) with the appropriate organometal derivative (e.g., organo-lithium, Grignard reagent). For example:
Protection strategies are required when using this method for preparation of certain oxazolidine-2,4-diones wherein R^" carries a substituent which is not compatible with organometallie reactions, e.g., an acyl group is protected as its ethylenic ketal. In 10 other cases, such as when R^" carries a group such as nitro or amino, this method generally lacks utility.
It will be evident to those skilled in the art that the preferred process for the oxazolidine-2,4-diones of the present invention will vary from one 15 given value of R^" to another, depending upon such factors as availability of starting materials,
yields, ability to remove undesirable impurities from the end-products, the chemical nature of the substituent groups contained in the final products, etc. 20 The pharmaceutically-acceptable cationic salts of the compounds of the present invention which form such salts are readily prepared by reacting the acid forms with an appropriate base, usually one equivalent, in a co-solvent. Typical bases are sodium hydroxide, 25 sodium methoxide, sodium ethoxide, sodium hydride, potassium methoxide, me^gnesium hydroxide, calcium hydroxide, benzathine, choline, diethanolamine, ethylenediamine, meglumine, benethamine, diethyl-amine, piperazine and tromethamine. Those salts 30 which do not precipitate directly are isolated by concentration to dryness or by addition of a
non-solvent. In some cases, salts can be prepared by mixing a solution of the acid with a solution of a different salt of the cation (sodium ethylhexanoate, magnesium oleate), employing a solvent in which the desired cationic salt precipitates, or can be otherwise isolated by concentration and addition of a non-solvent.
The pharmaceutically acceptable acid addition salts of the compounds of the present invention which form such salts are readily prepared by reacting the base forms with an appropriate acid, usually one equivalent, in a cosolvent. Typical acids are hydrochloric, hydrobromic, nitric, sulfuric, phosphoric, methanesulfonic, maleic, succinic, etc. Those salts which do not precipitate directly are isolated by concentration to dryness or by addition of a non-solvent.
3-Acylated derivatives of the present invention are readily prepared by using standard conditions of acylation, e.g. the reaction of the oxazolidine-2,4-dione salt (per se, or conveniently formed in situ by the addition of one equivalent of a tertiary amine such as triethylamine or N-methylmorpholine with an equivalent of the appropriate acid chloride or acid anhydride) or reaction of the oxazolidine-2,4-dione with the appropriate organic isocyanate, optionally in the presence of a catalytic amount of tertiary amine base. In either case, the reaction is carried out in a reaction inert solvent, such as toluene, tetrahydrofuran or methylene chloride. The temperature is not critical, and can be over a broad range (e.g. 0-150°C.). It will be evident to those skilled in the art that such acylation will be complicated by
' -V
rV
A
competing or even selective sidechain (R*) acylation when the sidechain contains a primary or secondary amine function.
It will be evident to those skilled in the art 5 that the compounds of the present invention are asymmetric and therefore capable of existing in two optically active enantiomeric forms. The racemic compounds of the present invention, being acids when R is H,
form salts with organic amines. These racemic forms 10 are therefore generally capable of resolution into the optically active forms by the classic method of forming diastereomeric salts with optically active amines, now separable by selective crystallization; alternatively those compounds containing a basic 15 amine function can be resolved by forming a salt with an optically active acid, preferrably a strong organic acid such as a sulfonic acid. In general, one of the enantiomeric forms is found to have greater activity than the other. 20 The reactions employed to prepare the compounds of this invention can generally be monitored by standard tic methods, employing commercially available plates. Suitable eluants are common solvents such as chloroform, ethyl acetate or hexane or suitable 25 combinations thereof which will differentiate starting materials, products, by-products, and in some cases intermediates. Applying these methods, which are well known in the art, will permit further improvement in the methodology of the specific examples detailed 30 hereinafter, e.g. the selection of more optimal reaction times and temperatures, as well as aid in the selection of optimal processes.
Th e oxazolidine-2,4-diones of the present invention are readily adapted to clinical use as antidiabetic agents. The hypoglycemic activity required for this clinical use is defined by the glucose 5 tolerance test procedure which follows. Intact male albino rats are the experimental test animals employed for such purposes. The test animals are fasted approximately 18-24 hours. The rats are weighed, numbered and recorded in groups of five or six as 10 needed. Each group of animals is then dosed intraperitoneal ly with glucose (one gram per kilogram) and orally with either water (controls) or compound (at a level usually selected from the range 0.1 to 100 mg/kg). Blood glucose levels (mg/100 ml.) are measured 15 in tail blood samples over a period of 3 hours in both control and treated groups. With equivalent zero hour blood glucose levels in control and treated groups, the % lowering of blood glucose at 0.5 hour, 1 hour, 2 hours and 3 hours is calculated as:
[Control Blood Glucose] - [Treated Blood Glucose] inna
[Control Blood Glucose] K
Clinically useful hypoglycemic agents show activity in this test. The hypoglycemic activities determined for compounds of the present invention are summarized 25 in Table I. This table records % blood glucose lowering at the 0.5 hour and 1 hour time points. A blood glucose lowering of 9% or greater generally reflects statistically significant hypoglycemic activity in this test. Those compounds which show significant 30 activity only at the 2 hour or 3 hour points have such activity recorded in footnotes.
-25-Table I
Hypoglycemic Activity of Oxazolidine-2,4-Diones in the Rat Glucose Tolerance Test
ArN^NH
Jj % Lowering
Dose of Blood
Glucose Level
AT
(mg./kq.)
0.5 hr.
1 hr.
2-Thienyl
11
8
-Benzoyl-
7
3-Bromo-
8
6(a)
-Bromo-
100
36
19
-Chloro-
100
26
17
3-Methoxy-
13
16
-Methoxy-
9
7
3-Methyl-
100
17
14
12
-Methyl
50
18
-Phenyl
50
1
(b)
3-Thienyl
23
17
4-Bromo-
100
31
14
9
4-Methoxy-
11
8
4-Methoxy-2-methyl-
16
14
4-Ethoxy-
19
19
4-Ethoxy-2-methyl-
7
12
4-Propoxy-
11
6
2-Furyl
100
27
23
11
7
3-Bromo-
18
11
11
-Bromo-
50
19
2
11
1 97
d
Table I. (Continued)
% Lowering
Ar
Dose (mq./kq.>
of Blood 0.5 hr.
Glucose Level 1 hr.
-Chloro-
21
3-Methoxy-
-Methyl-
100
27
19
-Phenyl-
6
4(c)
3-Fury1
17
13
14
8
2,5-Dimethyl-
100
33(e)
16(f)
4-Iodo-
19(e)
0(f)
3-Benzo[b]thienyl
100
11
7-Benzo[b]thienyl
100
-4
12(d)
7-Benzo[b]furanyl
-
-
-
-Chloro-
23(e)
(f)
8-Chromanyl
-
-
-
6-Chloro-
-
11
6-Fluoro-
-
9
2,3-Dihydrobenzo-furanyl
—
—
—
-Chloro-
-
23(g)
2-Pyrrolyl
100
11
8
1-Methyl-
100
18
17
1-Ethyl-
100
14
16
1-(1-Butyl)-
100
4
13
1-Phenyl
100
32
3-Indolyl
-
-
-
-Bromo-
100
9
1-Methyl-
100
11
8
Table I. (Continued)
% Lowering Dose of Blood Glucose Level
Ar (mg./kg.) 0.5 hr. 1 hr.
3-Pyridyl -
2-Methoxy 10 - 13
2-Ethoxy- 25 - 20
2-Methoxy-5-chloro- 25 22 17
2-Ethoxy-5-chloro- 10 - 24(g) 10 5-Quinolyl - - -
6-Methoxy- 20 - 7(h)
8-Quinolyl 18 19 16
6-Chloro- 10 - 16
6-Fluoro- 10 - 15
7-Methoxy- 10 - -(i)
2-Thiazolyl- 75 11 . 10
2-Benzthiazolyl- 50 8 10
-isoxazolyl - - -
3-Methyl- 100 4 7(j)
(a)
11
at 2 hours.
(b)
9
at 2 hours.
(c)
at 3 hours.
(d)
16
at 2 hours;
at
3
hours.
(e)
At
0.75 hours.
(f)
At
1.5 hours.
(g)
At
0.75 hours.
(h)
9
at 2 hours.
(i)
12
at 3 hours.
(j)
24
at 2 hours,
14
at
3
hours.
The oxazolidine-2,4-diones of the present invention are clinically administered to mammals, including man, via either the oral or the parenteral route. Administration by the oral route is preferred, 5 being more convenient and avoiding the possible pain and irritation of injection. However, in circumstances where the patient cannot swallow the medication, or absorption following oral administration is impaired, as by disease or other abnormality, it is essential 10 that the drug be administered parenterally. By either route, the dosage is in the range of about 0.10 to about 50 mg./kg. body weight of the subject per day, preferably about 0.20 to about 20 mg./kg.
body weight per day administered singly or as a 15 divided dose. However, the optimum dosage for the individual subject being treated will be determined by the person responsible for treatment, generally smaller doses being administered initially and thereafter increments made to determine the most suitable 20 dosage. This will vary according to the particular compound employed and with the subject being treated.
The compounds can be used in pharmaceutical preparations containing the compound, or pharmaceutical-ly acceptable acid salt thereof, in combination with 25 a pharmaceutically acceptable carrier or diluent.
Suitable pharmaceutically acceptable carriers include inert solid fillers or diluents and sterile aqueous or organic solutions. The active compound will be present in such pharmaceutical compositions in amounts 30 sufficient to provide the desired dosage amount in the range described above. Thus, for oral administration the compounds can be combined with a suitable solid or liquid carrier or diluent to form capsules, tablets,
powders, syrups, solutions, suspensions and the like. The pharmaceutical compositions can if desired,
contain additional components such as flavorants, sweeteners, excipients and the like. For parenteral 5 administration the compounds can be combined with sterile aqueous or organic media to form injectable solutions or suspensions. For example, solutions in sesame or peanut oil, aqueous propylene glycol and the like can be used, as well as aqueous solutions 10 of water-soluble pharmaceutically acceptable acid addition salts of the compounds. The injectable solutions prepared in this manner can then be administered intravenously, intraperitoneally, subcutaneously or intramuscularly, with intramuscular administration 15 being preferred in man.
The present invention is illustrated by the following examples. However, it should be understood that the invention is not limited to the specific details of these examples.
1 978
-30-EXAMPLE 1
Methyl 2-Methoxypyridine-3-carboxylate Thionyl chloride (50 ml.) was added to 2-methoxy-pyridine-3-carboxylic acid (5 g.) in 50 ml. of carbon tetrachloride and the mixture refluxed for 2 hours. The reaction mixture was cooled, evaporated to solids and chased with multiple portions of fresh carbon tetrachloride. The resulting acid chloride hydrochloride was dissolved in excess methanol (50 ml.), stirred for 16 hours at room temperature, then evaporated an oil and taken up in chloroform. The chloroform solution was washed with two portions of saturated sodium bicarbonate and then one portion of brine,
dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an oil [4.63 g.; pnmr/CDCl^/delta (ppm): 3.9 and 4.1 (2s, 6H), 6.9 (m, 1H), 8.2 (m, 2H)].
By the same procedure, 4-methylpyridine-3-carboxylic acid is converted to methyl 4-methylpyridine-3-carboxy-late.
1978 54
-31-EXAMPLE 2
3-Methanesulfinylmethylcarbonyl-2-Methoxypyridine Sodium hydride (2.69 g., 50% dispersion in oil, 0.056 mole) was washed three times with petroleum ether. Following the third decantation, traces of petroleum ether were removed by evaporation in vacuo. Dimethylsulfoxide (30 ml.) was added and the mixture heated in an oil bath at 75°C. for 45 minutes, by which time hydrogen evolution had ceased. The mixture was cooled in an ice-water bath and diluted with 30 ml. of dry tetrahydrofuran. Title compound of the preceding Example (4.63 g., 0.028 mole) in 10 ml. of dry tetrahydrofuran was added dropwise over 5 minutes. The reaction mixture was warmed and stirred at room temperature for 30 minutes, poured into 180 ml. of water, acidified to pH 4 with IN hydrochloric acid and extracted with three portions of chloroform. The combined organic layers were dried over magnesium sulfate, filtered and concentrated to yield title product as an oil [4.97 g.; pnmr/CDCl^/delta (ppm); 2.8 (s, 3H), 4.1 (s, 3H), 4.4 and 4.7 (2d, 2H), 7.0 (m, 1H), 8.3 (m,
2H) ] .
By the same procedure the 4-methyl compound of the preceding Example is converted to 3-methanesulfinyl-methylcarbonyl-4-methylpyridine.
EXAMPLE 3
S-Methyl 2-Acetoxy-2-(2-methoxy-3-pyridyl)-
thioacetate
Title compound of the preceding'Example (3.97 g.), sodium acetate (3.97 g.) and acetic anhydride (40 ml.) were combined in 80 ml. of toluene and heated at 115° for 16 hours. The mixture was cooled and evaporated to dryness in vacuo to yield crude product. The latter was chromatographed on 200 g. of silica gel with 2:1 chloroform:ethyl acetate as eluant, tic monitoring and collecting 10 ml. fractions. Clean product fractions 58-79 were combined and concentrated to an oil. To remove possible traces of residual acetic anhydride, the oil was taken into wet ethanol, held for 15 minutes, re-evaporated, chased with toluene taken up in chloroform, dried over anhydrous magnesium sulfate, filtered, and re-evaporated to yield the title product as an oil [3.16 g.; Rf 0.60 (3:1 ethyl acetate: methanol); m/e 255; ir (CH2Cl2) 1748, 1686, 1582, 1460, 1205 cm"1].
By the same procedure the methyl compound of the preceding Example is converted to S-methyl 2-acetoxy-2-(4-methyl-3-pyridyl)thioacetate.
EXAMPLE 4
-(2-Methoxy-3-pyridyl)oxazolidine-2,4-dione Sodium methoxide (632 mg., 11.7 mmoles) was taken into 50 ml. of absolute ethanol and the solution 5 cooled in an ice-water bath. Drea (234 mg., 3.9
mmole) was added, followed by the title compound of the preceding Example (1.0 g., 3.9 mmole) in 5 ml. of ethanol. The mixture was heated at reflux for 16 hours, then cooled to room temperature, neutralized 10 with 11.7 ml. of IN hydrochloric acid and evaporated to a gum which was chased with toluene. The gum was chromatographed on 40 g. of silica gel with 1:2 ethyl acetate:chloroform as eluant, tic monitoring and 10 ml. fractions collected. Product containing fractions 15 6-15 were combined and evaporated to a viscous oil,
which was crystallized from water [75 mg; m.p. 183-186°C., Rf 0.32 (1:2 ethyl acetate:chloroform)].
By the same method, the methyl analog of the preceding Example is converted to 5-(4-methyl-3-20 pyridyl)oxazolidine-2,4-dione.
197
EXAMPLE 5
Ethyl 2-Ethoxypyridine-3-carboxylate 2-Ethoxypyridine-3-carboxylic acid (4 g.) was converted to its acid chloride hydrochloride by reflux-5 ing with 8.6 ml. of thionyl chloride for 60 minutes. The reaction mixture was evaporated to solids with toluene chase to removed the excess thionyl chloride. The residue was taken into 80 ml. of ethanol and held for 16 hours at 0°C., then evaporated to solids, which 10 were partitioned between toluene and IN sodium hydroxide The aqueous layer was extracted with fresh toluene and the two organic layers combined, washed with water and then brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an 15 oil [3.2 g.; pnmr/CDCl3/delta (ppm) 1.6 (2s, 6H), 4.4-5.0 (2q, 4H), 7.2 and 8.2 (m, 3H)].
• 8 978 5 4
EXAMPLE 6 2-Ethoxy-3-methanesulfinylmethyl carbonylpyridine
Using methylene chloride in place of chloroform in the isolation, the procedure of Example 2 was employed to convert product of the preceding Example (3.0 g.) to title product [2.63 g.; m.p. 89-91°C.; pnmr/CDCl3/delta (ppm), 1.5 (t, 3H), 2.8 (s, 3H), 4.2-4.8 (s and q, 4H) , 6.8-7.1 and 8.0-8.4 (3H)].
EXAMPLE 7
S-Methyl 2-Acetoxy-2-(2-ethoxy-3-pyridyl)-
thioacetate
Using a reaction time of 4 hours at 100°C. and then 48 hours at room temperature, the procedure of Example 3 was employed to convert the product of the preceding Example (2.5 g.) to crude product, isolated as an oil by evaporation of the reaction mixture. The oil was taken up in ethyl acetate, washed in sequence with three portions of IN sodium hydroxide, one of water and one of brine, dried over anhydrous magnesium sulfate and evaporated to yield title product as an oil [2.96 g.; Rf 0.78 (10:1 ethyl acetate:methanol); m/e 269].
1978 5 4
-36-EXAMPLE 8
2-(2-Ethoxy-3-pyridyl)-2-hydroxyacetamide Product of the preceding Example (2.9 g.) was combined with 30 ml. of ethanol and 30 ml. of cone.
ammonium hydroxide, stirred at room temperature for 3 hours and then evaporated to yield crude product as an oil (2.7 g.). The oil was chromatographed on 170 g. of silica gel using ethyl acetate as eluant and tic monitoring. Clean product fractions were combined and 10 evaporated to yield title product as an oil [0.9 g.;
Rf 0.6 (10:1 ethyl acetate:methanol); pnmr/CDCl^/delta (ppm) 1.4 (t, 3H), 4.5 (q, 2H), 5.4 (s, 1H), 6.2-8.2 (m, 5H)].
11
-37-EXAMPLE 9
-(2-Ethoxy-3-pyridyl)oxazolidine-2, 4-dione Product of the preceding Example (900 mg., 4.6 mmole) was combined with 25 ml. of tert-butanol.
Dimethyl carbonate (1.08 g., 9.2 mmole) and then potassium tert-butoxide (1.03 g., 9.2 mmole) were added and the reaction mixture refluxed for 3.5 hours. The reaction mixture was cooled, poured into 10 ml. of IN hydrochloric hydrochloric acid, the pH adjusted to 10 7.0, and extracted with two portions of ethyl acetate.
The aqueous layer was saturated with salt and extracted with additional ethyl acetate. The three organic layers were combined, back-washed with a small portion of water and then brine, dried over anhydrous magnesium 15 sulfate and evaporated to yield crude product as a viscous oil. Purified title product was obtained by crystallization from toluene (295 mg., m.p. 140-143°C.; m/e 272).
Anal. Calcd. for: C_-.H.-O .N„ :
10 4 2
C, 54.05; H, 4.54; N, 12.61.
Found: C, 54.34, H, 4.85, N, 12.70.
EXAMPLE 10 Methyl 5-Chloro-2-methoxypyridine-3-
carboxylate
By the procedure of Example 1, 5-chloro-2-5 methoxypyridine-3-carboxylic acid [Sarges et al^. , J.
Med. Chem. 19, 709 (1976); 10 g.] was converted to its acid chloride, which was added in one portion to 150 ml. of methanol (slight exotherm), then made basic with triethylamine (approximately 1.1 equivalents). 10 The reaction mixture was evaporated to solids and the residue partitioned between ethyl acetate and water. The ethyl acetate layer was washed with fresh water and then brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product [9.75 g 15 m.p. 79-81°C.; pnmr/CDCl^/delta (ppm) 3.8 (s, 3H), 4.1 (s, 3H), 8.1 (d, 1H), 8.3 (d, 1H)].
EXAMPLE 11
-Chloro-3-methanesulfinylmethylcarbonyl-
2-methoxypyridine
By the procedure of Example 2, the product of the preceding Example (9.7 g., 0.045 mole) was converted to title product isolated as a visous oil (10.3 g., m/e 249/247).
• 9
978
EXAMPLE 12
S-Methyl 2-Acetoxy-2-(5-chloro-2-methoxy-3-
pyridyl)thioacetate
Using a reaction time of 19 hours at 100°C./ the 5 procedure of Example 3 and the isolation method of Example 7 were employed to convert product of the preceding Example (10.3 g.) to title product in the form of a viscous oil (8.8 g.; pnmr/CDCl^ includes singlet at 6.4; m/e 291/289). 10 EXAMPLE 13
2-(5-Chloro-2-methoxy-3-pyridyl)-2-hydroxy-
acetamide
Methanol (125 ml.) was saturated with anhydrous ammonia at 0-5°C. The product of the preceding Example 15 (8.8 g.) in 25 ml. of methanol was added and the reaction mixture stirred overnight at room temperature, then concentrated to a viscous oil (7.3 g.). The oil was chromatographed on 400 g. of silica gel using 1:1 chloroform:ethyl acetate as eluant, tic monitoring and 20 10 ml. fractions. Clean product fractions 190-270 were combined and evaporated to yield title product [1.3 g.; m.p. 110-113°C.; m/e 218/216; ir(KBr) 3444, 3410, 1684 cm"1].
*
| ^ ^/7 (^3)
^ u (a
EXAMPLE 14
-(5-Chloro-2-methoxy-3-pyridyl)oxazolidine-
2,4-dione
Using a reflux period of 15 hours, the procedure 5 of Example 9 was employed to convert the product of the preceding Example (1.25 g., 5.8 mmoles) to title product. To isolate, the reaction mixture was cooled to room temperature and the pH adjusted to 3 with IN hydrochloric acid. The mixture was then evaporated in 10 vacuo to slightly gummy solids, which gave filterable,
crude product on stirring with 25 ml. of water (1.09 g., m.p. 199-204°C. Recrystallization from 15 ml. of ethanol gave purified title product [470 mg.; m.p. 212-214°C.; m/e 244/242; ir(KBr) 3174, 3074, 2980, 15 1830, 1752 cm"1].
C5"? a r-
e V/ cj 5
EXAMPLE 15
2- (6-Chloro-8-quinolyl)-2-hydroxyacetamide Ethyl 2-(6-chloro-8-quinolyl)-2-hydroxyacetate (1.6 g.) in 300 ml. of conc. ammonium hydroxide was 5 heated to reflux. Since complete dissolution did not result, the reaction mixture was cooled, diluted with 5 0 ml. of ethanol and reheated to reflux for 0.5 hour. The reaction mixture was concentrted to a volume of 100 ml., cooled slowly and a crop of title product 10 (320 mg., m.p. 195-198°C.) recovered by filtration.
Additional product (145 mg). was recovered by concentration of the mother liguor to 50 ml. and extraction into three portions of ethyl acetate. The combined organic layers were washed with saturated sodium bi-15 carbonate, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness.
By the same procedure, ethyl 2-(6-chloro-2,3-dihydro-7-benzo[b]furanyl)-2-hydroxyacetate is converted to ethyl 2-(6-chloro-2,3-dihydro-7-benzo[b]furanyl)-2-20 hydroxyacetamide.
# H97B
EXAMPLE 16
-(6-Chloro-8-quinolyl)oxazolidine-2,4-dione Potassium tert-butoxide (292 mg., 2.6 mmoles) was dissolved in 20 ml. of tert-butanol. Dimethyl carbonate (234 mg. 2.6 mmoles) and then title compound of the preceding Example (300 mg., 1.3 mmoles) were added. The reaction mixture refluxed for 18 hours, then cooled to room temperature, adjusted to pH 3 with IN hydrochloric acid and diluted with IN hydrochloric acid and ethyl acetate. The aqueous layer was washed with two additional portions of ethyl acetate. The organic layers were combined, washed with two portions of fresh IN hydrochloric acid and then brine, dried over anhydrous magnesium sulfate, filtered and evaporated to an oil (130 mg.). Crystallization of the oil from isopropyl ether gave purified title product [58 mg., m.p. 207-210°C.; ir(KBr) 1839, 1825, 1740 cm"1].
By the same procedure the benzofuran analog of the preceding Example is converted to 5-(6-chloro-2,3-dihydro-7-benzo[b]furanyl)oxazolidine-2,4-dione.
EXAMPLE 17
2-(6-Fluoro-8-quinolyl)-2-hydroxyacetamide Ethyl 2-(6-fluoro-8-quinolyl)-2-hydroxyacetate (1.1 g.) was refluxed for 10 minutes in 300 ml. of 5 conc. ammonium hydroxide. The reaction mixture was cooled slightly, clarified by filtration and evaporated to solids. Trituration of the residue with 25 ml. of toluene gave the title product (8 60 mg., m.p. 169-171°C.) .
EXAMPLE 18
-(6-Fluoro-8-quinolyl)oxazolidine-2,4-dione Dsing a reflux period of 3.5 hours, the product of the preceding Example (840 mg., 3.8 mmoles) was converted to title product by the procedure of Example 15 16. In this case, a pH of 2 was used in the isolation . without addition of excess IN hydrochloric acid and the crude product was recrystallized from toluene [120 mg., m.p. 202-204°C.; m/e 246; ir(KBr) 1819, 1743, 1363 cm"1].
EXAMPLE 19
-(8-Quinolyl)oxazolidin-4-one-2-thione Potassium thiocyanate (484 mg., 4.9 mmoles) and potassium cyanide (370 mg., 5.7 mmoles) were combined 5 in 5 ml. of water and cooled to 0°C. Quinoline-8-
carbaldehyde [J. Org. Chem. 41, p. 957 (1976); 779 mg., 4.9 mmoles] was added, followed by the dropwise addition of hydrochloric acid (30%, 1.9 ml.). After stirring for 25 minutes at 0°C., the reaction mixture was 10 heated to 90-100°C. for 25 minutes, cooled, quenched into crushed ice, adjusted to pH 8 with sodium bicarbonate and extracted with cloroform. The organic layer was dried over anhydrous magnesium sulfate, filtered and evaporated to dryness (163 mg.). The latter was 15 partitioned between IN sodium hydroxide and ethyl acetate. The basic layer was acidified and extracted with fresh ethyl acetate. The two ethyl acetate layers were combined, dried, filtered and evaporated to yield title product [72 mg.; Rf 0.65 (ethyl acetate)]. 20 The original, pH 8 aqueous layer was salted and extracted with ethyl acetate to yield an additional crop (114 mg.). The last aqueous phase was acidified and extracted with ethyl acetate to yield a third crop (115 mg.).
By the same method, 7-chloroquinoline-8-carb-25 aldehyde is converted to 5-(7-chloro-8-quinolyl)oxazol idin-4-one-2-thione.
. 4
EXAMPLE 20
-(8-Quinolyl)oxazolidine-2,4-dione Title compound of the preceding Example (230 mg., 0.94 mmole) was taken into 6 ml. of 2:1 methanol:water 5 and cooled to 0°C. Bromine (0.07 ml., 21.7 mg., 2.7 mmoles) was added and the reaction mixture allowed to warm slowly to room temperature, then stirred for 1 hour. The reaction mixture was evaporated to dryness and the residue partitioned between IN sodium hydroxide 10 and ethyl acetate. The aqueous layer was separated,
acidified and extracted with two portions of fresh ethyl acetate. The acidic extracts were combined, dried and evaporated to an oil (144 mg.). Crystallization from toluene-chloroform and recrystallization from toluene 15 gave purified title product (40 mg., m/e 228).
Anal. Calcd. for: ci2Hg°3N2 . 0. 33H2O:
C, 61.54; H, 3.70; N, 11.96. Found: C, 61.50; H, 3.89; N, 11.52.
By the same method the chloro compound of the 20 preceding Example is converted to 5-(7-chloro-8-quinolyl)• oxazolidine-2,4-dione.
EXAMPLE 21 5-(6-Methoxy-5-quinolyl)oxazolidin-4-
' one-2-thione
By the procedure of Example 19, 6-methoxyquinoline-5 5-carbaldehyde (0.77 g.) was converted to title product.
After quenching into ice, a first crop (190 mg.) was isolated by extraction into ethyl acetate, drying over anhydrous magnesium sulfate and evaporation to dryness. A second crop (176 mg.) was isolated in like manner by 10 adjusting the aqueous phase to pH 8 with bicarbonate and extracting with additional ethyl acetate. Both crops had m/e 274. The second crop also had m/e 258, indicating contamination with the product of the next step.
EXAMPLE 22
-(6-Methoxy-5-quinolyi)oxazolidine-2,4-dione The combined product crops of the preceding Example (0.36 g., 1.31 mmole) were taken into 15 ml.
of methanol. Sodium metaperiodiate (0.56 g., 2.62
mmoles) in 7.2 ml. of 5% sodium bicarbonate was added dropwise. After stirring for 3 hours at room temperature, the reaction mixture was quenched with water, acidified and extracted with two portions of ethyl acetate. The 10 organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness (110 mg.). The aqueous phase was adjusted to pH 7 and further crude product (100 mg.) obtained by extraction with ethyl acetate. The crude crops were combined, 15 taken into IN sodium hydroxide, acidified to pH 4 with acetic acid and extracted with fresh ethyl acetate. The latter organic extracts were combined and evaporated to dryness. Trituration of the residue with ether, allowing the mixture to stand until crystal-20 lization was complete, gave title product (34 mg.; m.p. 144-146°C.).
EXAMPLE 23 5-(7-Methoxy-8-quinolyl)oxazolidin-4-one-2-thione
By the procedure of Example 19, but using adjust-5 ment to pH 7 with bicarbonate after quench and ethyl acetate for extraction, 7-methoxyquinoline-8-carb-aldehyde (2.0 g., 10.7 mmoles) was converted to title product [1.17 g.; Rf 0.7 (2:1 ethyl acetate:chloroform)]. This product was not partitioned between 10 aqueous base and ethyl acetate, nor was a second crop isolated by salting the aqueous phase and further extracting.
EXAMPLE 24
-(7-Methoxy-8-quinolyl)oxazolidine-2,4-dione 15 Product of the preceding Example (0.74 g., 2.7
mmoles) was combined with 30 ml. of methanol and 15 ml. of 5% sodium bicarbonate. Sodium metaperiodate (1.15 g., 5.4 mmoles) in 15 ml. of water was added dropwise. After stirring for 3 hours at room temperature, 20 the reaction mixture was quenched with water, acidified to pH 2-3 and extracted with two portions of ethyl acetate. The extracts were combined, dried and evaporated to dryness (360 mg.). Recrystallization from water gave purified title product (100 mg.; m.p. 25 207-208°C.).
Anal. Calcd. for . 1. 2H20:
C, 59.40; H, 4.34; N, 10.66. Found: C, 59.33; H, 4.01; N, 10.66.
'ird' StzJ,
P1 *
EXAMPLE 25
-Hydroxy-5-(l-methyl-2-pyrrolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione Alloxan hydrate (3.2 g., 0.02 mole) was dissolved 5 in 50 ml. of ethanol by warming. 1-Methylpyrrole
(1.6 g., 0.02 mole) was added and the mixture warmed for 5 minutes on a steam bath, while perfusing with hydrogen chloride. After standing at room temperature for 0.5 hour, the reaction mixture was evaporated to 10 dryness and the residue triturated with water to yield title product as a solid [2.9 g.; m/e 223; Rf 0.5 (1:1 ethyl acetate:hexane/5% acetic acid)].
EXAMPLE 26
-(l-Methyl-2-pyrrolyl)oxazolidine-2,4-dione 15 Product of the preceding Example (2.8 g.) was combined with 25 ml. of IN sodium hydroxide and heated on a steam bath for 30 minutes, by which time complete dissolution had occurred. On acidification, a gum precipitated, which solidified on trituration with 20 water (1.2 g.). Recrystallization from methanol-ether afforded purified title product [0.70 g.; m.p. 108-114 (dec); m/e 180].
Anal. Calcd. for CgHgO^: C, 53.33; H, 4.48; N, 15.55. Found: C, 53.16; H, 4.72; N, 15.28.
0
EXAMPLE 27 5-Hydroxy-5-(l-ethyl-2-pyrrolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione
Potassium pyrrole [J. Chem. Soc., p. 52 (1931);
1 g.; 0.01 mole] was slurried in 5 ml. of tetrahydrofuran. Ethyl iodide (1 ml., 0.012 mole) was added, a slight exotherm being noted. The mixture was stirred for 0.5 hour, heated to reflux for 0.5 hour, cooled to room temperature, diluted with 15 ml. of water and extracted with 10 ml. of ether. The ether extract was washed with 5 ml. of water, then added to alloxan hydrate (1.6 g.) which had been dissolved in 25 ml. of ethanol by heating. The ether was boiled off and the ethanolic residue refluxed for 0.5 hour, then evaporated to a water-soluble gum. The gum was taken up in 25 ml. of ethyl acetate, washed with two 10 ml. portions of water and re-evaporated to yield title product as a gum (0.6 g., m/e 237).
)7 S3 £*
i/
v_>
EXAMPLE 28
-(l-Ethyl-2-pyrrolyl)oxazolidine-2,4-dione The procedure of the preceding Example was repeated on a three times scale. The initially isolated 5 product gum (0.03 mole of the pyrimidinetrione) was stirred with 60 ml. of IN sodium hydroxide for 0.5 hour, then acidified with conc. hydrochloric acid and extracted with ethyl acetate. The extract was filtered from insoluble impurities, and concentrated to a gum 10 (2.2 g.). The gum was chromatographed on 100 ml. of silica gel with (1:1 ethyl acetate:hexane as eluant and tic monitoring. Early fractions contained the desired product; these were combined and evaporated to an oil which crystallized on standing. Trituration with water 15 gave purified title product (170 mg.; m.p. 90-93°C.; m/e 194).
Anal. Calcd. for .0.25H20:
C, 54.40; H, 5.32; N, 14.10. Found: C, 54.37; H, 5.16; N, 13.76.
EXAMPLE 29 5-Hydroxy-5-[1-(1-butyl)-2-pyrrolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione Potassium pyrrole (3.0 g., 0.03 mole), 1-iodo-5 butane (9.2 g., 0.05 moles) and 10 ml. of tetrahydrofuran were combined and refluxed for 1.5 hours by which time the reaction mixture had become a thick mass. The reaction mixture was diluted with 30 ml. of water and extracted with 35 ml. of ether. The ether was back-10 washed with water, then added to a solution of anhydrous alloxan (4.8 g., 0.03 mole) obtained by heating in 50 ml. of ethanol. The ether was distilled away, 6N hydrochloric acid (5 ml., 0.03 mole) was added, and the mixture refluxed for 3 minutes, cooled, evaporated 15 to a gum, and triturated with water to afford title product [5.1 g.; m.p. 135 (dec); m/e 265].
1 97
■T55
O
EXAMPLE 30
-[1-(1-Butyl)-2-furyI]oxazolidine-2,4-dione
Product of the preceding Example (5.1 g., 0.019
mole) was combined with IN sodium hydroxide (38 ml.,
0.038 mole) and stirred at room temperature for 10
minutes. The reaction mixture was filtered, washed with ether, cooled in an ice-water bath, acidified with conc. hydrochloric acid and extracted with three portions of ethyl acetate. The organic extracts were
combined, washed with brine, dried over anhydrous sodium sulfate and evaporated to gummy solids. The latter was chromatographed on silica gel with ethyl acetate as eluant and tic monitoring to yield partially purified product isolated as an oil (950 mg.). The
latter was rechromatographed using 1:1 ethyl acetate:
hexane as eluant, yielding purified title product as an oil [0.59 g.; m/e 222; Rf 0.72 (ethyl acetate)].
Anal. Calcd. for C.. . H. .0oNo. 0. 5H_0:
11 14 3 2 2
C, 57.38; H, 6.57; N, 12.17. 20 Found: C, 57.40; H, 6.35; N, 12.15.
# 197
-54-EXAMPLE 31
Sodium 5-[1-(1-butyl)-2-furyl]oxazolidine-
2,4-dione
Product of the preceding Example (370 mg., 1.66 5 mmoles) was dissolved in 5 ml. of methanol. Sodium bicarbonate (90 mg., 1.66 mmoles) was added. The resulting solution was evaporated to dryness and the solid residue triturated with ether to yield the title product [300 mg.; m.p. 123-126°C. (dec); tic mobility 10 with 1:1 ethyl acetate:hexane/5% acetic acid as eluant identical with the free base form].
• 197
EXAMPLE 32
-Hydroxy-5-(l-phenyl-2-pyrrolyl)-2,4,6-
(1H,3H,5H)pyrimidinetrione
1-Phenylpyrrole (1.4 g., 0.01 mole), alloxan
hydrate (1.6 g., 0.01 mole) and 50 ml. of ethanol were combined and refluxed for 15 minutes. No reaction was noted by tic. IN Hydrochloric acid (10 ml., 0.01
mole) was added and the acidified mixture refluxed for
minutes. Incomplete reaction was noted by tic. A
second portion of alloxan hydrate (1.6 g., 0.01 mole)
was added and the mixture refluxed another 15 minutes,
cooled and evaporated to dryness. Trituration of the residue with water gave title product [2.3 g.; m/e
285; m.p. 232-234°C. (dec); Rf 0.3 (1:1 ethyl acetate:
hexane)].
Anal. Calcd. for C.. .H110ilN_.0.25Ho0:
14 11 4 3 2
C, 58.01; H, 4.00; N, 14.50. Found: C, 57.84; H, 4.05; N, 14.56.
197854
EXAMPLE 33
-(l-Phenyl-2-pyrrolyl)oxazolidine-2,4-dione The product of the preceding Example (1 g.) was heated on a steam bath for 20 minutes with 20 ml. of IN sodium hydroxide. The mixture was then cooled in an ice-water bath, acidified with conc. hydrochloric acid and the supernatant decanted from the resulting ^^immy precipitate. The gum was taken up in ethyl acetate, washed with water, and evaporated to an oil (0.47 g.). The agueous decant was also extracted with ethyl acetate, the extract back washed with water and evaporated to a second oil (0.28 g.). The two oils ^kre combined, chromatographed on 150 ml. of silica gel with 1:1 ethyl acetate:hexane as eluant and tic monitoring. The early, product fractions were combined, evaporated to an oil (410 mg.) and the oil crystallized from ether-hexane to yield purified title product [280 mg.; m.p. 130-132°C.; m/e 242; Rf 0.47 (1:1 ethyl acetate:hexane)].
Anal. Calcd. for C, 64.46; H, 4.16; N, 11.57.
Found: C, 64.40; H, 4.35; N, 11.56.
EXAMPLE 34
-Hydroxy-5-(1-methyl-3-indolyl)-2,4,6,-
1H, 3H,5H)pyrimidinetrione
Alloxan hydrate (1.6 g., 0.01 mole) 1-methylindole (1.3 g., 0.01 mole) and ethanol (50 ml.) were combined and the mixture refluxed for 0.5 hour, then concentrated to half-volume, diluted with water and the resulting product recovered by filtration [2.7 g., Rf 0.5 (1:1 ethyl acetate:hexane/5% acetic acid)].
EXAMPLE 35
-(l-Methyl-3-indolyl)oxazolidine-2,4-dione Product of the preceding Example (2 g.) was heated on a steam bath for 15 minutes with 35 ml. of IN sodium hydroxide. The reaction mixture was cooled to room temperature, acidified to pH 1 with conc. hydrochloric acid, and decanted from a small amount of gum (130 mg.). The decant was clarified by filtration, cooled in an ice-water bath, and the resulting solids (330 mg.) recovered by filtration. The filtrate was extracted with ethyl acetate; the extract was back-washed with water and evaporated to solids (0.61 g.). The solid products were combined and recrystallized from ethyl acetate/hexane to yield title product (0.33 g.; m.p. 152-153.5°C.).
Anal. Calcd. for ® :
C, 61.99; H, 4.45; N, 12.05 Found: C, 61.99; H, 4.45; N, 12.02
1 978 54
EXAMPLE 36 5-Hydroxy-5-(5-bromo-3-indolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione Alloxan hydrate (1.6 g., 0.01 mole) was dissolved in 40 ml. of ethanol by heating. 5-Bromoindole (1.96 g., 0.01 mole) was added and heating near reflux continued for 15 minutes. Tic did not indicate that reaction had occured. IN Hydrochloric acid (10 ml.) was then added while maintaining the reaction near reflux.
After 10 minutes, the reaction was concentrated to wet solids. Trituration of these wet solids with water gave the title product [3.17 g., m.p. 250°C.; Rf 0.45 (1:1 ethyl acetate:hexane/5% acetic acid); Rf 0.3 (1:5 ethyl acetate:hexane/5% acetic acid)].
EXAMPLE 37
-(5-Bromo-3-indolyl)oxazolidine-2,4-dione Product of the preceding Example (3.1 g.) was heated on a steam bath with 50 ml. of IN sodium hydroxide for 15 minutes, then cooled and crude product (1.25 g.) precipitated by acidification with conc. hydrochloric acid. Chromatography on silica gel,
using 1:1 ethyl acetate:hexane as eluant and tic monitoring gave purified title product [0.41 g.; m.p. 185-189°C.; Rf 0.55 (1:5 ethyl acetate:hexane/5%
acetic acid)].
Anal. Calcd. for C^H^O^^Br: C, 44.76; H, 2.38; N, 9.49. Found: C, 45.10; H, 2.68; N, 9.58.
EXAMPLE 38 5-Hydroxy-5-(2-thiazolyl)-2,4,6-(1H,3H,5H)pyrimidinetrione Thiazole (1.7 g., 0.02 mole) was dissolved in 5 tetrahydrofuran (35 ml.) and cooled to -60°C. Butyl-lithium (9 ml. of 2.4M in hexane, 0.0216 mole) was added dropwise over 2 0 minutes, and the reaction mixture stirred for an additional 30 minutes at -60°C. In this manner 2-thiazolyllithium was formed. Anhydrous 10 alloxan (3 g., 0.021 mole) was dissolved in 20 ml. of tetrahydrofuran and added dropwise over 20 minutes, keeping the temperature at -60°C. The stirred reaction mixture was warmed to room temperature over 30 minutes, then recooled to 0°C. IN Hydrochloric acid (25 ml.) 15 was added portion wise and the quenched reaction mixture extracted with 50 ml. of ethyl acetate. The ethyl acetate extract was back-washed with 15 ml. of water, dried over anhydrous sodium sulfate, filtered and evaporated to yield title product [1.9 g.; m/e 20 227; Rf 0.4 (1:1 ethyl acetate:hexane/5% acetic acid)].
By the same procedure, oxazole is converted to 5-hydroxy-5-(2-oxazolyl)-2,4,6-(lH,3H,5H)pyrimidinetrione.
EXAMPLE 39
-(2-Thiazolyl)oxazolidine-2,4-dione Title product of the preceding Example (1.37 g.) was stirred at room temperature with 24 ml. of IN 5 sodium hydroxide. The reaction mixture was allowed to stand for 25 minutes, acidified with 3 ml. of glacial acetic acid and extracted with two 50 ml. portions of ethyl acetate. The extracts were separately dried over sodium sulfate, filtered and evaporated to solids, 10 the first yielding 184 mg., the second 85 mg. These solids were combined and chromatographed on 50 ml. of silica gel with 1:1 ethyl acetate:hexane/5% acetic acid as eluant and tic monitoring. Clean product fractions were combined, evaporated to dryness and the 15 residue triturated with hexane to yield purified title product (155 mg.; m.p. 150-152°C.).
Anal. Calcd. for C^O^S: C, 39.13; H, 2.19; N, 15.21. Found: C, 39.53; H, 2.52; N, 14.95.
By the same procedure, the other product of the 20 preceding Example is converted to 5-(2-oxazolyl)oxa-zolidine-2,4-dione.
j ^ fr
^ /> / k: 3
EXAMPLE 40 5-Hydroxy-5-(2-benzthiazolyl>-2,4,6-(1H,3H,5H)pyrimidinetrione By the procedure of Example 38, benzthiazole 5 (2.7 g., 0.02 moles) was converted to its 2-lithio derivative and then reacted with anhydrous alloxan to yield title product, initially isolated as an oil. The latter was crystallized from ether-hexane [2.2 g.; Rf 0.55 (1:1 ethyl acetate:hexane/5% acetic acid)]. 10 EXAMPLE 41
-(2-Benzthiazolyl)oxazolidine-2,4-dione Product of the preceding Example 2.15 g.) was stirred with 30 ml. of IN sodium hydroxide for 30 minutes. The reaction mixture was extracted with 15 ether and product (0.46 g.) precipitated by acidification of the aqueous layer with 6N hydrochloric acid. Chromatography on 50 ml. of silica gel with 1:1 ethyl acetate:hexane/5% acetic acid as eluant and tic monitoring, followed by recrystallization from acetone-20 isopropyl ether gave purified title product [110 mg., m.p. 214-216°C. (dec)].
Anal. Calcd. for C..-H^O-N.S: C, 51.29; H, 2.58; N, 11.96.
1U D 3 C
Found: C, 51.51; H, 2.99; N, 12.21.
EXAMPLE 42
2-(6-Chloro-8-chromanyl)-2-trimethylsiloxy-
ethanenitrile 6-Chlorochroman-8-carbaldehyde (7 g., 0.036 mole) 5 in 70 ml. of methylene chloride was cooled to 0-5°C.
Zinc iodide (100 mg.) was added, followed by the drop-wise addition of trimethylsilylcarbonitrile (4.26 g., 0.043 mole). The reaction mixture was stirred at room temperature for 64 hours, then washed in sequence with 10 three portions of saturated sodium bicarbonate and one of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an oil [9.5 g.; ir(CH CI ) 2857, 1479, 1215, 1190, 1060
-1
cm ] .
EXAMPLE 43
Ethyl 1-(6-Chloro-8-chromanyl)-1-hydroxy-methanecarboximldate Hydrochloride To cold (0-5°C.), saturated ethanolic hydrogen chloride (250 ml.) there was added, in a dropwise 20 manner, product of the preceding Example (9.29 g.) in 15 ml. of ethanol, keeping the temperature below 10°C. The mixture was stirred at 0-5°C. for 35 minutes and then evaporated to an oil. Crystallization from ethanol-ether gave title product [5.7 g.; m.p. 125-25 127° (dec); m/e 271/269].
* /)
-63-EXAMPLE 44
-(6-Chloro-8-chromanyl)oxazolidine-2,4-dione Product of the preceding Example (5.4 g., 18.6 mmoles) was suspended in 250 ml. of tetrahydrofuran, 5 cooled in an ice-water bath, and triethylamine (6.01 g., 0.06 mole) added. The cold mixture was perfused with phosgene for 30 minutes, stirred at room temperature for 1 hour and then poured into 1 liter of crushed ice. The quenched reaction mixture was extracted with 10 three portions of methylene chloride. The combined extracts were washed with brine, dried over anhydrous magnesium sulfate and evaporated to solids. The residue was recrystallized from toluene to yield purified title product (3.28 g., m.p. 170-172°C., m/e 15 269/267).
Anal. Calcd. for C12H1()04NC1: C, 53.84; H, 3.77; N, 5.23 Found: C, 53.73; H, 3.83; N, 5.48
EXAMPLE 45
2-(6-Fluoro-8-chromanyl)-2-trimethylsiloxy-
ethanenitrile
By the procedure of Example 42, 6-fluorochroman-8-carbaldehyde (3.2 g., 0.0178 mole) was converted to title product as an oil [4.51 g., m/e 279; ir (CHC12) 1498, 1205, 1066 cm"1].
EXAMPLE 46
Ethyl 1-(6-Fluoro-8-chromanyl)-1-hydroxy-methanecarboxlmidate Hydrochloride Using a reaction time of 1 hour at 0-5°C., the procedure of Example 43 was employed to convert product of the preceding Example (4.4 g.) to title product [4.1 g.; m.p. 124-126°C. (dec); m/e 253].
EXAMPLE 47
-(6-Fluoro-8-chromanyl)oxazolidine-2,4-dione By the procedure of Example 44, product of the preceding Example (3.9 g., 0.01,34 mole) was converted to crude title product. Crude solids were taken into IN sodium hydroxide and extracted with two portions of ether. Product was reprecipitated by adding the basic aqueous layer slowly to excess 3N hydrochloric acid. Recrystallization from toluene gave purified title product [2.73 g.; m.p. 174-176°C.; m/e 251],
Anal. Calcd. for C-^H-^C^NF: C, 57.37; H, 4.01; N, 5.58 Found: C, 57.74; H, 3.91; N, 5.40
I 97
EXAMPLE 48
2-(5-Chloro-2,3-dihydro-7-benzo[b]furanyl)-2-
' trimethylsiloxyethanenitrile
-Chloro-2,3-dihydrobenzo[b]furan-7-carbaldehyde 5 (900 mg., 4.9 mmoles) was dissolved in 25 ml. of ether. Zinc iodide (20 mg.) and then trimethylsilylcarbonitrile (970 mg., 9.8 mmoles) were added and the mixture stirred 16 hours at room temperature, then diluted with 50 ml. ether, washed with three portions 10 of saturated sodium bicarbonate and one of brine,
dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an oil [1.4 g.; m/e 283/281; ir(CHCl2) 1479, 1457, 1435, 1180, 866, 848 cm"1].
By the same method 5-fluoro-2,3-dihydrobenzo[b]-
furan-7-carbaldehyde is converted to 2-(5-fluoro-2,3-dihydro-7-benzo[b]furanyl)-2-trimethylsiloxyethane-nitrile.
7
EXAMPLE 49
Ethyl 1-(5-Chloro-2,3-dihydro-7-benzo[b]-furanyl)-1-hydroxymethanecarboximidate Hydrochloride
By the procedure of Example 43, title compound of the preceding Example (1.37 g.) was converted to title product. The initially isolated solids were repulped twice in ether to obtain purified product [1.28 g.; m.p. 149-152°C. (dec); m/e 257/255; ir(KBr) 3162, 10 2875, 1650, 1524, 1458 cm"1].
By the same method the fluoro compound of the preceding Example is converted to ethyl l-(5-fluoro-2,3-dihydro-7-benzo[b]furanyl)-1-hydroxymethanecarbox-imidate hydrochloride. 15 EXAMPLE 50
-(5-Chloro-2,3-dihydro-7-benzo[b]furanyl)- oxazolidine-2,4-dione
By the procedure of Example 44, title compound of the preceding Example (1.1 g.) was converted to toluene 20 recrystallized title product [630 mg.; m.p. 197-
199°C.; m/e 255/253; ir(KBr) 3084, 1833, 1810, 1746
-1.
cm ] .
By the same procedure the fluoro analog of the preceding Example is converted to 5-(5-fluoro-2,3-25 dihydro-7-benzo[b]furanyl)oxazolidine-2,4-dione.
EXAMPLE 51
2-(3-Methyl-5-isoxazolyl)-2-trimethylsilyl-
ethanenitrile
By the procedure of Example 42, 3-methylisoxazole-5-carbaldehyde (3.4 g., 0.032 mole) was converted to title product, isolated as an oil (6.5 g., no aldehyde proton by nmr).
By the same method, isothiazole-5-carbaldehyde is converted to 2-(5-thiazolyl)-2-trimethylsilylethane-nitrile and 5-methylisoxazole-3-carbaldehyde (Kane et al., Japan 62/17,572) is converted to 2-(5-methyl-3-isoxazolyl)-2-trimethylsilylethanenitrile.
EXAMPLE 52
Ethyl 1-Hydroxy-l-(3-methyl-5-isoxazolyl)-
methanecarboximidate Hydrochloride
Title product of the preceding Example (6.5 g.) was dissolved in cold, saturated ethanolic hydrogen chloride (50 ml.) and held at 5°C. for 16 hours.
Title product was recovered by filtration (3.3 g., m.p. 119-121°C.).
By the same method, the other products of the preceding Example are converted to ethyl 1-hydroxy-l-(5-isothiazolyl)methanecarboximidate hydrochloride and ethyl 1-hydroxy-l-(5-methyl-3-isoxazolyl)methanecarboximidate hydrochloride.
EXAMPLE 53
-(3-Methyl-5-isoxazoiyi)oxazoiidine-2,4-dione By the procedure of Example 44, title product of the preceding Example (2.2 g.), was converted to title 5 product. After quench into crushed ice, the product was extracted into ether, the combined extracts dried and evaporated to an oil (1.4 g.). Further extraction with ethyl acetate and evaporation gave additional oil (0.4 g.). The oils were combined and partitioned 10 between 25 ml. of IN sodium hydroxide and 25 ml. of ether. The basic aqueous phase was separated, acidified with conc. hydrochloric acid and extraced with 25 ml. of ethyl acetate. The ethyl acetate extract was back-washed with water, evaporated to dryness, the 15 residue triturated with ether (146 mg., m.p. 173-175°C.). The ether triturate was evaporated to dryness and triturated with fresh ether (238 mg., m.p. 175-177°C.).
By the same method, the other products of the 20 preceding Example are converted to 5-(5-isothiazolyl)-oxazolidine-2,4-dione and 5-(5-methyl-3-isoxazolyl)-oxazolidine-2,4-dione.
s
EXAMPLE 54
-(5-Chloro-2-ethoxy-3-pyridyl)oxazolidine-
2,4-dione
-(2-Ethoxy-3-pyridyl)oxazolidine-2,4-dione (125 mg.) was suspended in 100 ml. of water and dissolved by warming to 56°C. Chlorine was bubbled into the warm solution for 30 minutes, during which time the temperature slowly dropped to 34°C. and a precipitate formed. The reaction mixture was flushed with nitrogen for 30 minutes and crude product recovered by filtration (101 mg., m.p. 119-124°C.). Two recrystallizations from 2:1 ethanol:water gave purified title product [24 mg.; m.p. 145-147°C.; Rf 0.56 (1:1 ethyl acetate: chloroform); m/e 256].
By the same procedure, substituting 10% fluorine in nitrogen, 5-(2-ethoxy-3-pyridyl)oxazolidine-2,4-dione is converted to 5-(5-fluoro-2-ethoxy-3-pyridyl)-oxazolidine-2,4-dione.
^ / C.?
EXAMPLE 55
2-(3-Furyl)-2-Trimethylsiloxyethanenitrile To a mixture of 3-furaldehyde (1.92 g., 20 mmoles) and about 100 mg. of zinc iodide in 25 ml. of ether, 5 trimethylsilylcarbonitrile (4.74 g., 48 mmoles) was added dropwise. The mixture was stirred about 16 hours at room temperature. The reaction mixture was washed sequentially with saturated sodium bicarbonate, water and brine, dried over anhydrous sodium sulfate, 10 filtered and evaporated in vacuo to yield 2-(3-furyl)-
2-trimethylsiloxyethanenitrile [2.2 g.; pnmr/CDCl^/delta: 0.2 (s, 9H); 5.4 (s, 1H); 6.4 (m, 1H); 7.3 (m, 1H) ;
7.5 (m, 1H)]
EXAMPLE 56
Ethyl 1-Hydroxy-l-(3-furyl)-
methanecarboximidate Hydrochloride 2-(3-Furyl)-2-trimethylsiloxyethanenitrile (1.0 g.) was dissolved in 10 ml. of saturated ethanolic hydrogen chloride at 0-5°C. The resulting solution 20 was held at about 5°C. for 16 hours. The reaction mixture was concentrated to about half volume and diluted with ether. Filtration, with ether wash, gave ethyl 1-hydroxy-l-(3-furyl)methanecarboximidate hydrochloride (746 mg.; m.p. 113-115°C.; m/e 169).
EXAMPLE 57 5-(3-Furyl)oxazolidine-2,4-dione Ethyl 1-hydroxy-l-(3-furyl)methanecarboximidate hydrochloride (1.5 g., 7.5 mmoles) was combined with 5 50 ml. of tetrahydrofuran and triethylamine (2.21 g., 21.9 mmoles) and cooled to 10°C. Phosgene was bubbled through the cooled reaction mixture for 20 minutes.
After stirring the mixture for an additional 30 minutes, nitrogen was flushed through the mixture for 10 minutes. 10 The reaction mixture was poured slowly into 100 g. of crushed ice. The product was extracted into two portions of ether and crude product isolated as an oil by evaporation. The oil was taken up in 5 ml. of IN sodium hydroxide and extracted with ether. The basic 15 aqueous phase was acidified and extracted with fresh ether. Product was isolated as a gummy solid (600 mg.) by evaporation of the latter ether extract. Trituration with chloroform afforded purified 5-(3-furyl)oxazolidine-2,4-dione (109 mg.; m.p. 86-88°C.; m/e 167). Addition 20 of hexane to the chloroform triturate gave a second crop of product (66 mg.; m.p. 86-88°C., m/e 167). Analysis: Calcd. for C^H^O^N:
C, 50.31; H, 3.01; N, 8.38.
Found: C, 49.97; H, 3.13; N, 8.37. 25 EXAMPLE 58
2-(5-Chloro-2-furyl)-2-trimethylsiloxyethanenitrile 5-Chloro-2-furaldehyde (2.7 g., 21 mmoles) was dissolved in 30 ml. of ether. Trimethylsilylcarbo-30 nitrile (6.3 ml., 50 mmoles) and zinc iodide (about
50 mg.) were added and the mixture stirred for 1.5 hours at room temperature, at which time tic (hexane:ethyl acetate 8:1) indicated complete reaction. Concentration to dryness afforded 2-(5-chloro-2-furyl)-2-35 trimethylsiloxyethanenitrile as an oil (5.5 g.;
pnmr/CDCl^/delta: 0.3 (s, 9H); 5.4 (s, 1H); 6.1 (d, 1H); 6.5 (d, 1H)] .
EXAMPLE 59 Ethyl 1-(5-chloro-2-furyl)-1-hydroxymethanecarboximidate Hydrochloride 2-(5-Chloro-2-furyl)-2-trimethylsiloxyethanenitrile 5 (2.3 g.) was dissolved in saturated ethanolic hydrogen chloride (25 ml.) at 0°C. The solution was held for 2.5 hours at about 5°C. and then concentrated to oil. Trituration with 20 ml. of ether afforded crystalline ethyl 1-(5-chloro-2-furyl)-1-hydroxymethanecarboximidate 10 hydrochloride (1.2 g.; m.p. 112-114°C.; m/e 203).
EXAMPLE 60
-(5-Chloro-2-furyl)oxazolidine-2,4-dione Ethyl 1-(5-chloro-2-furyl)-1-hydroxymethanecarboximidate hydrochloride (1.2 g., 5 mmoles) was suspended 15 in 50 ml. of tetrahydrofuran and cooled in an ice bath. Following the addition of triethylamine (2.1 ml., 15 mmoles), phosgene was bubbled into the reaction mixture for 20 minutes, maintaining the temperature at 10 to 20°C. The mixture was flushed with nitrogen and 20 poured slowly into 100 ml. of crushed ice. The quenched reaction mixture was extracted with 100 ml. of ether, and the ether back-extracted with brine and concentrated to an oil. The oil was taken up in 15 ml. of fresh ether, the solution clarified and 25 extracted with 10 ml. of IN sodium hydroxide. The basic extract was acidified with concentrated hydrochloric acid and product extracted into ethyl acetate. After back extracting with water, the ethyl acetate layer was concentrated to an oil (550 mg.). A portion 30 of this oil (500 mg.) was chromatographed on about 5 0 ml. of silica gel, with 5:1 hexane:ethyl acetate containing 5% acetic acid as eluant. The column was
monitored by tic (same eluant). Late eluted, product containing fractions were combined, evaporated to dryness and triturated with hexane, affording 5-(5-chloro-2-furyl)oxazolidine-2,4-dione [177 mg.; m.p.
112-114°C.; m/e 201; 0.25 (5:1 hexane:ethyl acetate with 5% acetic acid)].
Analysis: Calcd. for C^H^O^NCl:
C, 41.71; H, 2.00; N, 6.95.
Found: C, 41.80; H, 2.21; N, 6.77. 10 EXAMPLE 61
2-(5-Bromo-2-furyl)-2-trimethylsiloxyethanenitrile 5-Bromo-2-furaldehyde (1.1 g., 6 mmoles) was dissolved in 50 ml. of ether. A catalytic quantity (about 50 mg.) of zinc iodide was added and then 15 trimethylsilylcarbonitrile (746 mg., 1.2 equiv.) was added dropwise. The reaction was monitored by ir (disappearance of typical carbonyl absorption) and pnmr (disappearance of typical aldehyde proton peak). After 60 minutes at room temperature, the reaction 20 mixture was washed with saturated sodium bicarbonate, twice with water, and finally with brine, dried over anhydrous sodium sulfate and evaporated to yield 2-(5-bromo-2-furyl)-2-trimethylsiloxyethanenitrile as an oil [1.2 g.; pnmr/CDCl^/delta: 0.3 (s, 9H); 5.6 (s, 25 1H); 6.4 (d, 1H); 6.6 (d, 1H)].
EXAMPLE 62 Ethyl l-(5-Bromo-2-furyl)-1-hydroxymethanecarboximidate Hydrochloride Following the procedure of Example 56, except that 5 the reaction mixture was not concentrated prior to addition of ether, 2-(5-bromo-2-furyl)-2-trimethyl-siloxyethanenitrile (1.2 g.) was converted to ethyl 1-(5-bromo-2-furyl)-1-hydroxymethanecarboximidate hydrochloride (480 mg., m.p. 120-122°C., m/e 247, 10 249). A less pure second crop (235 mg., m.p. 104-106°C.) was recovered by evaporation of mother liquor and trituration of the residue with ether.
EXAMPLE 63
-(5-Bromo-2-furyl)oxazolidine-2,4-dione 15 Ethyl 1-(5-bromo-2-furyl)-1-hydroxymethanecarbox-
imidate hydrochloride (982 mg., 3.4 mmoles) was converted to 5-(5-bromo-2-furyl)oxazolidine-2,4-dione [126 mg., m.p. 126-129°C., m/e 245, 247, Rf 0.2 (5:1 hexane:ethyl acetate with 5% acetic acid)] by the 20 procedure of Example 57.
EXAMPLE 64
2-(3-Bromo-2-furyl)-2-trimethylsiloxyethanenitrile By the procedure of Example 55, 3-bromo-2-furaldehyde (1.75 g., 10 mmoles) in 50 ml. of ether was reacted 25 with trimethylsilylcarbonitrile (8.8 ml., 70 mmoles)
in the presence of about 100 mg. of zinc iodide. At the end of the 16 hour reaction period, the ether supernatant was decanted from solids and evaporated to dryness to yield 2-(3-bromo-2-furyl)-2-trimethylsiloxy-30 ethanenitrile [3 g., R^ 0.7 (3:1 hexane:ethyl acetate)].
;"7 ^
EXAMPLE 65 Ethyl 1-(3-Bromo-2-furyl)-1-hydroxymethanecarboximidate Hydrochloride 2-(3-Bromo-2-furyl)-2-trimethoxysilylethanenitrile 5 (6.8 g.) was dissolved in 70 ml. of saturated ethanolic hydrogen chloride at 0°C. and maintained at about 5°C. for 2 hours. Concentration to dryness and trituration with acetone afforded ethyl 1-(3-bromo-2-furyl)-1-hydroxymethanecarboximidate hydrochloride [4.4 g., 10 m.p. 117-119° (dec.)].
EXAMPLE 66
-(3-Bromo-2-furyl)oxazolidine-2,4-dione By the procedures of Example 60, except that phosgene was bubbled into the reaction mixture at 0 to 15 10°C., ethyl 1-(3-bromo-2-furyl)-1-hydroxymethane-
carboximidate hydrochloride (4.4 g.) was converted to purified 5-(3-bromo-2-furyl)oxazolidine-2,4-dione [847 mg.; m.p. 128-130°C.; 0.20 (5:1 hexane:ethyl acetate containing 5% acetic acid)].
Analysis: Calcd. for C^H^O^NBr:
C, 34.16; H, 1.63; N, 5.69.
Found: C, 34.30; H, 1.88; N, 5.67.
7
O
-76-EXAMPLE 67
2-(2-Furyl)-2-trimethylsiloxyethanenitrile 2-Furaldehyde (24 g., 0.25 mole) was cooled to 0-5°C., zinc iodide (500 mg.) was added and the 5 mixture stirred. Trimethylsilylcarbonitrile (30 ml.) was added dropwise. The mixture was allowed to warm to room temperature and stirred for approximately 64 hours at room temperature. The reaction mixture was diluted with methylene chloride, extracted twice 10 with saturated sodium bicarbonate, dried over anhydrous magnesium sulfate, treated with activated carbon,
filtered and evaporated to yield 2-(2-furyl)-2-trimethylsiloxyethanenitrile as an oil [36 g., 74%; pnmr/CDCl^/ delta: 0.2 (s, 9H); 5.6 (s, 1H); 6.4 (m, 1H); 6.6 (m, 15 1H); 7.4 (d, 1H)].
EXAMPLE 68
Ethyl 1-(2-Furyl)-1-hydroxymethanecarboximidate Following the procedure of Example 56, 2-(2-furyl)-2-trimethylsiloxyethanenitrile (15 g.) was 20 reacted with saturated ethanolic hydrogen chloride,
except that a reaction time of about two hours was employed. Crude product was isolated by evaporating the reaction mixture to an oil. The oil was partitioned in 400 ml. of chloroform and saturated sodium 25 bicarbonate. The chloroform was washed twice with fresh saturated sodium bicarbonate, washed once with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to yield ethyl 1-(2-furyl)-1-hydroxymethanecarboximidate as an oil [10.6 g., 81%; 30 pnmr/CDCl3/delta: 1.3 (t, 3H); 4.1 (q, 2H); 5.1 (s, 1H); 4.8-5.2 (m, 1H); 6.3 (m, 2H); 7.3 (d, 1H)].
%
EXAMPLE 69
-(2-Furyj)oxazolidine-2,4-dione Ethyl 1-(2-furyl)-1-hydroxymethanecarboximidate (10.5 g., 6.2 mmoles) was dissolved in 125 ml. of 5 stirring tetrahydrofuran and cooled to 0-5°C. Triethyl-amine (12.5 g., 0.124 mole) was added and the cold solution then perfused with phosgene for 35 minutes, warmed to room temperature and stirred for an additional 16 hours. The reaction mixture was slowly poured into 10 1 liter of ice and water. The product was extracted into 3 portions of ethyl acetate. The extracts were combined and product extracted into 4 portions of IN sodium hydroxide. The combined aqueous extracts were acidified with 6N hydrochloric acid, and product 15 extracted into 4 portions of chloroform. The combined chloroform extracts were dried over anhydrous magnesium sulfate, treated with activated carbon, filtered and evaporated to yield crude product as an oil (2.1 g.). Column chromatography on 100 g. of silica gel with 2:1 20 chloroform:ethyl acetate as eluant in 10 ml. fractions, monitored by tic, gave, by evaporation of fractions 36-48, purified 5-(2-furyl)oxazolidine-2,4-dione (281 mg.; m.p. 99-102°C.; m/e 167). Recrystallization from toluene gave more highly purified product (235 mg., 25 m.p. 101-103°C.).
Analysis: Calcd. for C^H^O^N:
C, 50.31; H, 3.02; N, 8.38.
Found: C, 50.41; H, 3.25; N, 8.28.
EXAMPLE 70 5-Hydroxy-5-(3-methoxy-2-furyl) -2,4,6(1H,3H,5H)-pyrimidinetrione 3-Methoxyfuran (3.5 g., approximately 50% pure 5 from Preparation 10), alloxan hydrate [5,5-dihydroxy-2,4,6(1H,3H,5H)-pyrimidinetrione, 4.8 g.] and 75 ml. of ethanol were combined and refluxed for 1 hour. The reaction mixture was cooled to room temperature and concentrated to dryness. Trituration of the residue o
with 25 ml. of water afforded 5-hydroxy-5-(3-methoxy-2-furyl)-2,4,6(1H,3H,5H)-pyrimidinetrione [1.9 g., m.p. 120-130 (dec.), m/e 240].
EXAMPLE 71
-(3-Methoxy-2-furyl)oxazolidine-2,4-dione 15 5-Hydroxy-5-(3-methoxy-2-furyl)-2,4,6{1H,3H,5H) -
pyrimidinetrione (1.7 g.) was stirred with IN sodium hydroxide (14 ml., 14 mmoles) for 20 minutes. The reaction mixture was acidified with acetic acid and product extracted into ethyl acetate and isolated in 20 crude form by evaporation to an oil. Chromatography on ca. 100 ml. of silica gel, monitored by tic,
afforded 5-(3-methoxy-2-furyl)oxazolidine-2,4-dione [470 mg., m.p. 10 2-104°C., 0.6 (1:1 hexane:ethyl acetate with 5% acetic acid)]. 25 EXAMPLE 72
2- ( 5-Phenyl-2-thienyl) -.2-trimethylsiloxyethanenitrile 5-Phenyl-2-thenaldehyde (0.9 g.) in 35 ml. of ether was reacted with 1 ml. of trimethylsilylcarbo-30 nitrile in the presence of about 50 mg. of zinc iodide. After 1 hour of stirring at room temperature, tic indicated reaction was complete. Evaporation to dryness gave 2-(5-phenyl-2-thienyl)-2-trimethylsiloxyethanenitrile [1.65 g., R^ 0.5 (5:1 hexane:ethyl 35 acetate with 5% acetic acid)].
EXAMPLE 73 Ethyl 1-Hydroxy-1-(5-phenyl-2-thienyl)-methanecarboximidate Hydrochloride 2-(5-Phenyl-2-thienyl)-2-trimethylsiloxyethane-5 nitrile (1.6 g.) was dissolved in 30 ml. of cold,
saturated ethanolic hydrogen chloride and maintained at 0 to 5°C. for about 17 hours. The reaction mixture was evaporated to dryness and triturated with ethyl acetate to yield ethyl 1-hydroxy-l-(5-phenyl-2-thienyl) 10 methanecarboximidate hydrochloride [0.9 g.; pnmr/DMSO/
delta: includes 1.1 (3H); 4.0 (2H); 5.2 (1H); 6.5 (1H)].
EXAMPLE 74
-(5-Phenyl-2-thienyl)oxazolidine-2,4-dione 15 Ethyl 1-hydroxy-l-(5-phenyl-2-thienyl)methane carboximidate hydrochloride (790 mg., 2.6 mmoles) and triethylamine (1.4 ml., 10 mmoles) were reacted with phosgene and product isolated according to the procedures of Example 12, except that the eluant in the 20 chromatography was 2:1 ethyl acetate:hexane, affording
-(5-phenyl-2-thienyl)oxazolidine-2,4-dione (172 mg., m.p. 233-235°C.).
Analysis: Calcd. for C^H^O^NS:
C, 60.23; H, 3.50; N, 5.40.
Found: C, 59.94; H, 3.65; N, 5.38.
EXAMPLE 75
2-(2-Thienyl)-2-trimethylsiloxyethanenitrile By the procedure of Example 67, 2-thenaldehyde (56.1 g., 46.8 ml., 0.5 mole) was reacted for 16 hours 30 with trimethylsilylcarbonitrile (60 ml.) in the presence of zinc iodide (approximately 0.5 g.),
yielding 2-(2-thienyl)-2-trimethylsiloxyethanenitrile as an oil [92 g.; m/e 211; pnmr/CDCl3/delta: 0.2 (s, 9H); 5.8 (s, 1H); 6.9-7.5 (m, 3H)].
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-80-EXAMPLE 76
Ethyl 1-Hydroxy-l-(2-thienyl)methanecarboximidate 2-(2-Thienyl)-2-trimethylsiloxyethanenitrile (45 g.) was dissolved in 450 ml. of absolute ethanol.
The solution was cooled to 0-5°C. and perfused with hydrogen chloride for 40 minutes. The mixture was kept at about 5°C. for 16 hours and evaporated to dryness. The residue was triturated with four 200 ml. portions of ether, and then partitioned between 400 ml. 10 of methylene chloride and saturated sodium bicarbonate. The organic phase was washed twice with saturated sodium bicarbonate, treated with activated carbon, filtered and concentrated to yield ethyl 1-hydroxy-l-(2-thienyl)methanecarboximidate as an oil which 15 solidified on standing [10 g.; pnmr/CDCl^/delta: 1.2
(t, 3H); 4.1 (q, 2H); 5.2 (s, 1H), 5.9 (s, 1H); 6.8-7.3 (m, 3H); 7.3-8.1 (s, 1H)].
EXAMPLE 77
-(2-Thienyl)oxazolidine-2,4-dione Ethyl 1-hydroxy-l-(2-thienyl)methanecarboximidate (10 g., 5.4 mmoles) and triethylamine (15.1 ml., 5 10.8 mmoles) were dissolved in 100 ml. of tetrahydrofuran. The solution was cooled to 0-5°C. and perfused with phosgene for 45 minutes. Stirring was continued for an additional 5 hours at 0-5°C. The reaction mixture was poured slowly over 1500 ml. of crushed 10 ice. The product was extracted into 1.1 liter of ethyl acetate in three portions. The combined ethyl acetate extracts were then extracted twice with saturated sodium bicarbonate and once with 1:1 saturated sodium carbonate:water. The combined bicarbonate and 15 carbonate washes were acidified to pH 1-2 with 6N
hydrochloric acid and product extracted into several portions of ether. The combined ether extracts were washed with brine, dried over anhydrous magnesium sulfate, treated with activated charcoal, filtered and 20 evaporated to yield product (3.0 g.). Recrystallization from toluene afforded 5-(2-thienyl)oxazolidine-2,4-dione (1.8 g.; m.p. 138-140°C., m/e 183).
Analysis: Calcd. for C^H^NO^S:
C, 45.89; H, 2.75; N, 7.65.
Found: C, 45.99; H, 2.87; N, 7.62.
EXAMPLE 78
2-(3-Methyl-2-thienyl)-2-trimethylsiloxyethanenitrile Following the procedure of Example 67, 3-methyl-2-thenaldehyde (31.6 g., 0.25 mole) was reacted with trimethylsilylcarbonitrile (30 ml.) for 16 hours in the presence of 500 mg. of zinc iodide. The reaction mixture was diluted with 200 ml. of methylene chloride and further isolated also according to Example 13, affording 2-(3-methyl-2-thienyl)-2-trimethylsiloxyethanenitrile [52 g., 93%; pnmr/CDCl3/delta: 0.2 (s, 9H); 2.3 (s, 3H); 5.7 (s, 1H); 6.8 (d, 1H); 7.25 (d,
1H)] .
EXAMPLE 79 Ethyl l-Hydroxy-l-(3-methyl-2-15 thienyl)methanecarboximidate
2-(3-Methyl-2-thienyl)-2-trimethylsiloxyethanenitrile (13 g.) was added dropwise to 100 ml. of cold ethanol, saturated with hydrogen chloride, keeping the temperature at 0-4°C. After 1 hour at 0-4°C., the 20 reaction mixture was evaporated to dryness. The residue was triturated three times with 100 ml.
portions of ether, and then partitioned between 300 ml. of methylene chloride and saturated sodium bicarbonate. The separated methylene chloride layer was washed with 25 two additional portions of saturated sodium bicarbonate, dried over anhydrous magnesium sulfate, filtered and evaporated to yield ethyl 1-hydroxy-l-(3-methyl-2-thienyl)methanecarboximidate (8.0 g., 69%; m.p. 73-76°C.; m/e 199).
9? a
EXAMPLE 80
-(3-Methyl-2-thienyj)oxazolidine-2,4-dione Ethyl 1-hydroxy-l-(3-methyl-2-thienyl)methanecarboximidate (6.0 g., 0.03 mole) was dissolved in 5 7 5 ml. of tetrahydrofuran and cooled to 0-5°C. Triethyl-
amine (6.07 g., 8.37 ml., 0.06 mole) was added, the solution was perfused with phosgene for 35 minutes, and poured slowly into 1 liter of ice and water. The product was extracted into three portions of ethyl 10 acetate. The ethyl acetate extracts were combined and product extracted into four portions of saturated sodium bicarbonate. The combined aqueous extracts were acidified with 6N hydrochloric acid and product reextracted into 3 portions of fresh ethyl acetate. 15 The combined fresh organic extracts were dried over anhydrous magnesium sulfate, filtered, and evaporated to yield product as an oil (2.4 g., 41%), which crystallized on scratching. Recrystallization from toluene gave purified 5-(3-methyl-2-thienyl)oxazolidine-20 2,4-dione (1.84 g., 31% overall; m.p. 119-121°C., m/e 197) .
Analysis; Calcd. for CgH^O^NS:
C, 48.72; H, 3.58; N, 7.10.
Found: C, 48.65; H, 3.58; N, 7.01.
A second crop of product (0.63 g.) was obtained by extraction of the initial ethyl acetate extracts with 3 portions of IN sodium hydroxide, followed by further isolation as above.
1 97 8
EXAMPLE 81 2-(5-Methyl-2-thienyl)-2-trimethylsiloxyethanenitrile 5-Methyl-2-thenaldehyde (25 g., 0.2 mole), zinc iodide (266 mg.) and 100 ml. of ether were combined and stirred at room temperature. Trimethylsilylcarbonitrile (23.5 g., 0.24 mole) was added dropwise and the reaction mixture stirred for an additional 2 hours. The reaction mixture was diluted with 100 ml. of ether, washed wtih two 50 ml. portions of 5% sodium bicarbonate, washed with two 25 ml. portions of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to produce 2-(5-methyl-2-thienyl)-2-trimethylsiloxyethanenitrile [42 g.; pnmr/CDCl^/delta: 0.2 (s, 9H); 2.2 (s, 3H); 5.6 (s, 1H); 6.6-7.4 (m,
2H) ] .
EXAMPLE 82 Ethyl 1-Hydroxy-l-(5-methyl-2-thienyl)-methanecarboximidate Hydrochloride With cooling to 0-5°C., ethanol (550 ml.) was saturated with hydrogen chloride. 2-(5-Methyl-2-thienyl)-2-trimethylsiloxyethanenitrile (42 g.) was dissolved in portions and the solution maintained at 0°C. for 2.5 hours. The reaction mixture was evaporated to dryness and the residue triturated with diethyl ether to provide ethyl 1-hydroxy-l-(5-methyl-2-thienyl)-methanecarboximidate hydrochloride [33 g.; m.p. 122-123°C., pnmr/DMSO/delta: 1.1-1.6 (3H); 2.5 (3H); 4.6 (2H); 5.9 (1H); 6.6-72 (2H)].
# 197
EXAMPLE 83
-(5-Methyl-2-thienyl)oxazolidine-2,4-dione Ethyl 1-hydroxy-l-(5-methyl-2-furyl)methanecarboximidate hydrochloride (10 g., 0.042 mole) was 5 combined with triethylamine (14.1 g., 0.14 mole) in 250 ml. of tetrahydrofuran and cooled to 0-5°C. The cold reaction mixture was perfused with phosgene for 30 minutes, warmed to room temperature and poured portionwise onto about 275 ml. of crushed ice. The 10 product was extracted into two 200 ml. portions of ethyl acetate. The ethyl acetate extracts were combined and extracted with two 150 ml. portions of IN sodium hydroxide. The combined agueous extracts were acidified with hydrochloric acid and then extracted 15 with two 250 ml. portions of fresh ethyl acetate. The last, combined organic extracts were dried over anhydrous magnesium sulfate, filtered and evaporated to yield 5-(5-methyl-2-thienyl)oxazolidine-2,4-dione (7.2 g.). Recrystallization from chloroform/hexane 20 gave purified product (910 mg.; m.p. 108-109°C.; m/e 197) .
7
EXAMPLE 84
2- (5-Chloro-2-thienyl)-2-trimethylsiloxyethanenitrile 5-Chlorothenaldehyde (5 g., 34 mmoles) was combined with zinc iodide (50 mg.) and 30 ml. of diethyl ether 5 and cooled to 0°C. Trimethylsilylcarbonitrile (4.04 g., 4 0 mmoles) was added dropwise and the reaction mixture warmed to room temperature and stirred for 4 hours. Additional equal portions of trimethylsilylcarbonitrile and zinc iodide were added and the reaction stirred an 10 additional 16 hours. The reaction mixture was diluted with ether, washed with two 30 ml. portions of 5%
sodium bicarbonate, washed once with 30 ml. of brine,
dried over anhydrous magnesium sulfate and evaporated to yield 2-(5-chloro-2-thienyl)-2-trimethylsiloxyethane-15 nitrile as an oil [4.0 g., pnmr/CDCl^/delta: 0.3 (s, 9H); 5.7 (s, 1H); 7.0 (q, 2H)].
By the same method, 3-fluoro-2-thenaldehyde, 4-fluoro-2-thenaldehyde, 5-fluoro-2-thenaldehyde, 5-fluoro-3-thenaldehye [Gronowitz and Rosen, Chem. Ser. 20 1, pp. 33-43 (1971); Chem. Abstracts 75, 20080c], 4-fluoro-3-thenaldehyde, 4-methoxy-3-thenaldehyde, and 4-methylthio-3-thenaldehyde are converted, respectively, to 2-(3-fluoro-2-thienyl)-2-trimethylsiloxyethanenitrile, 2-(4-fluoro-2-thienyl)-2-trimethylsiloxyethanenitrile, 25 2-(5-fluoro-2-thienyl)-2-trimethylsiloxyethanenitrile, 2-(5-fluoro-3-thienyl)-2-trimethylsiloxyethanenitrile, 2-(4-fluoro-3-thienyl)-2-trimethylsiloxyethanenitrile, 2-(4-methoxy-3-thienyl)-2-trimethylsiloxyethanenitrile, 2-(4-methylthio-3-thienyl)-2-trimethylsiloxyethanenitrile.
1 ©7 n
EXAMPLE 85 Ethyl 1-(5-Chloro-2-thienyl)-l-hydroxymethanecarboximidate Hydrochloride 2-(5-Chloro-2-thienyl)-2-trimethylsiloxyethanenitrile (4 g.) was dissolved in absolute ethanol (100 ml.). The solution was cooled to 0-5°C. and saturated with hydrogen chloride. The reaction mixture was held for 16 hours at 0°C., evaporated to dryness and triturated with ether to yield solid ethyl l-(5-chloro-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride [3 g., pnmr/DMSO/delta: 1.2 (3H); 4.2 (2H); 5.3 (1H); 6.6 (1H); 6.9 (1H); 7.4 (1H); 8.4 (1H)].
By the same method, the other nitriles of the preceding Example are converted to ethyl l-(3-fluoro-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride, ethyl 1-(4-fluoro-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride, ethyl l-(5-fluoro-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride, ethyl 1—(5— fluoro-3-thienyl)-1-hydroxymethanecarboximidate hydrochloride, ethyl 1-(4-fluoro-3-thienyl)-1-hydroxymethanecarboximidate hydrochloride, ethyl 1-hydroxy-l-(4-methoxy-3-thienyl)methanecarboximidate hydrochloride and 1-hydroxy-l-(4-methylthio-3-thienylmethanecarbox-imidate hydrochloride.
1
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EXAMPLE 86
-(5-Chloro-2-thienyl)oxazolldine-2,4-dione Ethyl 1-(5-chloro-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride (3.0 g., 12 mmoles) and 5 triethylamine (4.0 g., 39 mmoles) were combined in 90 ml. of tetrahydrofuran and cooled to 0°C. The slurry was perfused with phosgene for 30 minutes,
warmed to room temperature and stirred for 16 hours. The reaction mixture was poured slowly into 100 ml. 10 of crushed ice and product extracted into two 100 ml.
portions of ethyl acetate. The combined ethyl acetate extracts were back-washed with two 50 ml. portions of water and one 50 ml. portion of saturated sodium chloride, dried over anhydrous magnesium sulfate, 15 filtered and evaporated to a semi-solid (2.5 g.).
Recrystallization from toluene provided purified 5—(5— chloro-2-thienyl)oxazolidine-2,4-dione (0.6 g., m.p. 126-130°C.).
Analysis; Calcd. for C^H^O^NCIS:
C, 38.64; H, 1.84; N, 6.44.
Found: C, 38.17; H, 2.07; N, 6.91.
By the same method the other imino ethers of the preceding Example are converted to 5-(3-fluoro-2-thienyl)oxazolidine-2,4-dione, 5-(4-fluoro-2-thienyl)-25 oxazolidine-2,4-dione, 5-(5-fluoro-2-thienyl)oxazolidine-2,4-dione, 5-(5-fluoro-3-thienyl)oxazolidine-2,4-dione, 5-(4-fluoro-3-thienyl)oxazolidine-2,4-dione, 5-(4-methoxy-3-thienyl)oxazolidine-2,4-dione and 5—(4— methylthio-3-thienyl)oxazolidine-2,4-dione.
1 97 H r
-89-EXAMPLE 87
2-(4-Bromo-3-thienyl)-2-trimethylsiloxyethanenitrile 4-Bromo-3-thenaldehyde (5.5 g., 29 mmoles) in 75 ml. of methylene chloride was cooled to 0-5°C.
Zinc iodide (50 mg.) was added, followed by the dropwise addition of trimethylsilylcarbonitrile (3.47 g., 35 mmoles) over a 3 minute period. The mixture was warmed to room temperature, stirred for 16 hours, washed twice with saturated sodium bicarbonate, 10 washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 2-(4-bromo-3-thienyl)-2-trimethylsiloxyethanenitrile as an oil (7.6 g., 90%, m/e 291/289).
EXAMPLE 88
Ethyl 1-(4-Bromo-3-thienyl)-
1-hydroxymethanecarboximidate 2-(4-Bromo-3-thienyl)-2-trimethylsiloxyethanenitrile (7.5 g.) in 200 ml. of ethanol, cooled in an ice bath, was perfused with hydrogen chloride for 45 minutes. 20 After an additional 20 minutes at 0-5°C. the reaction mixture was evaporated to dryness and triturated with ether to yield the hydrochloride salt of the product as a hygroscopic solid. The salt was taken up in a mixture of methylene chloride and saturated sodium 25 bicarbonate. The separated methylene chloride layer was washed twice with saturated sodium bicarbonate,
washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield ethyl l-(4-bromo-3-thienyl)-1-hydroxymethanecarboximidate as an 30 oil (6.1 g., 89%, m/e 265/263).
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EXAMPLE 89
- (4-Bromo-3-thieny1) oxazol idine-2,4-dione Ethyl 1-(4-bromo-3-thienyl)-1-hydroxymethanecarboximidate (6.0 g., 23 mmoles) and triethylamine 5 (5.15 g., 51 mmoles) were combined in 250 ml. of tetrahydrofuran, cooled in an ice-water bath and perfused with phosgene for 35 minutes. The reaction mixture was warmed to room temperature, stirred for 1.5 hours, poured slowly over 1 liter of crushed ice, 10 and product extracted into 3 portions of methylene chloride. The combined methylene chloride extracts were evaporated to an oil, crystallized by the addition of a small amount of ether and hexane, and triturated in about 40 ml. of ether to yield 5-(4-bromo-3-thienyl)-15 oxazolidine-3,4-dione (3.4 g., 56%; m.p. 158-161°C.). Recrystallization from 40 ml. of toluene afforded purified product (2.51 g.; m.p. 164-166°C.; m/e 263/261).
Alternatively, the ether solution of the lithium derivative of 3,4-dibromothiophene is reacted with a 20 1.05 equivalent of alloxan according to the procedure of Example 54, yielding 5-(4-bromo-3-thienyl)-5-hydroxy-2,4,6(lH,3H,5H)-pyrimidinetrione. Following the procedure of Example 55, the latter is converted to the desired 5-(4-bromo-3-thienyl)oxazolidine-2,4-25 dione.
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EXAMPLE 90
2-(3-Thienyl)-2-trimethylsiloxyethanenitrile 3-Thenaldehyde (10 g., 0.089 moles), zinc iodide (12 0 mg.) and ether (60 ml.) were combined and stirred.
Trimethylsilylcarbonitrile (10.6 g., 0.107 mole) was added dropwise over 10 minutes and the reaction mixture stirred for 16 hours, diluted with 60 ml. of ether,
washed with two 30 ml. portions of 5% sodium bicarbonate, washed with 30 ml. of brine, dried over anhydrous 10 magnesium sulfate, filtered and evaporated to yield 2-(3-thienyl)-2-trimethylsiloxyethanenitrile as an oil [14.3 g., pnmr/CDCl3/delta: 0.2 (9H); 5.6 (1H); 7.0-7.5 (3H)].
EXAMPLE 91
Ethyl 1-Hydroxy-l-(3-thienyl)methanecarboximidate
At 0-5°C., 2-(3-thienyl)-2-trimethylsiloxyethanenitrile (14.3 g.) was dissolved portionwise in 500 ml. of ethanol, previously saturated with hydrogen chloride at 0-5°C. The solution was held at 0°C. for 16 hours, 20 and the product isolated as the hydrochloride salt by evaporation of the reaction mixture to dryness and trituration of the residue with ether. The salt was taken up in 400 ml. of chloroform and 100 ml. of saturated sodium bicarbonate. The separated chloroform 25 layer was washed with an additional 100 ml. of saturated sodium bicarbonate, washed with brine, dried over magnesium sulfate, filtered and evaporated to yield ethyl 1-hydroxy-l-(3-thienyl)methanecarboximidate [12.5 g., pnmr/CDCl^/delta: 1.0-1.3 (3H); 4.8-5.3 30 (2H); 5.0 (1H); 6.9-7.2 (3H), 7.3-8.0 (1H)].
EXAMPLE 92 5-(3-Thienyl)oxazolidine-2,4-dione Ethyl 1-hydroxy-l-(3-thienyl)methanecarboximidate (12.5 g., 0.067 mole) and triethylamine (16.1 g., 0.159 mole) were combined in 6 00 ml. of tetrahydrofuran and cooled to 0°C. The mixture was perfused with phosgene for 30 minutes, warmed to room temperature and allowed to stand for 16 hours. The mixture was poured slowly into 600 ml. of ice and water (foaming of excess phosgene), and extracted twice with, 600 ml. portions of ethyl acetate. The combined extracts were washed with two 300 ml. portions of IN sodium hydroxide The combined basic extracts were acidified with hydrochloric acid and product re-extracted into two fresh 300 ml. portions of ethyl acetate. The combined fresh extracts were dried over anhydrous magnesium sulfate, filtered and evaporated to solids (8.0 g.). Recrystal-lization from hot toluene gave purified 5-(3-thienyl)-oxazolidine-2,4-dione (5.5 g., m.p. 133-136°C.). A second recrystallization, from ethyl acetate/hexane, provided additional purification (first crop: 2.352 g. m.p. 136-138°C., m/e 183; ir (KBr): 5.5, 5.8 microns).
EXAMPLE 93 Ethyl 2-Hydroxy-2-(3-thienyl)acetate 3-Thenaldehyde (10 g., 0.089 mole) and sodium bisulfite (13.8 g., 0.133 mole) were heated at 50-60°C., 5 in 152 ml. of water for 2 hours, forming the bisulfite adduct _in situ. The reaction mixture was cooled to 5°C., and 200 ml. of ethyl acetate was added. To the stirred, two phase system, potassium cyanide (17.4 g., 0.267 mole) in 75 ml. of water was added dropwise over 10 30 minutes. The reaction mixture was warmed to 20°C.
and held for 1 hour. Additional potassium cyanide (5.7 g., 0.088 mole) was added and the mixture stirred an additional 10 minutes at 20°C. The layers were separated and the aqueous layer washed with 50 ml. of 15 ethyl acetate. The combined ethyl acetate layers were washed with saturated sodium chloride, providing a clean solution of the cyanohydrin of 3-thenaldehyde in ethyl acetate.
The solution of the cyanohydrin of 3-thenaldehyde 20 in ethyl acetate was stirred at room temperature and charged with 41.6 g. (52.7 ml., 10 equiv.) of ethanol and concentrated hydrochloric acid (15.2 ml., 0.182 mole) and the mixture refluxed for 17 hours. The reaction mixture was cooled to 25°C., washed with 100 ml. of 25 water and then with saturated sodium bicarbonate to a pH >7.0, dried over anhydrous magnesium sulfate,
treated with activated carbon, filtered and evaporated to an oil (approximately 11.5 g.) which upon addition of 46 ml. of 1:1 toluene/isooctane afforded crystalline 30 ethyl 2-hydroxy-2-(3-thienyl)acetate (7.4 g., 45%,
m.p. 55-57°C.).
EXAMPLE 94 2-Hydroxy-2-(3-thienyl)acetamide Ethyl 2-hydroxy-2-(3-thienyl)acetate (168 g., 0.9 03 mole) was slurried in 15N ammonium hydroxide 5 (4 20 ml., 6.3 moles) and heated to reflux for 2.5 hours. The resulting solution was cooled to 70°C. and toluene (840 ml.) was added. The stirred mixture was allowed to cool to 20°C. and granulated for 1 hour. Filtration, with toluene wash, gave 2-hydroxy-2-(3-thienyl)acetamide 10 (105.9 g., 75%, m.p. 120-126°C.). A second crop
(10.3 g., m.p. 114-120°C.) was obtained by evaporating the aqueous layer of the filtrate to 50 ml. and granulating with 100 ml. of toluene. Recrystallization of the first and second crops from ethyl acetate afforded a 15 77-79% recovery of purified product (m.p. 127-130°C.).
EXAMPLE 95 5-(3-Thienyl)oxazolidine-2,4-dione At 25°C., 2-hydroxy-2-(3-thienyl)acetamide (10.0 g., 0.064 mole) was added to a solution of 20 sodium methoxide (10 g., 0.185 mole) and diethyl carbonate (22.0 ml., 0.182 mole) in 200 ml. of ethanol. The reaction mixture was heated to reflux for 3 hours, cooled to 20°C. , and slowly diluted with 100 ml. of water. Ethanol was removed by evaporation 25 and the aqueous residue treated with activated carbon and filtered. The filtrate was layered with ethyl acetate and the pH adjusted to 1.0 with concentrated hydrochloric acid. The aqueous layer was separated and washed with 100 ml. of ethyl acetate. The combined 30 ethyl acetate layers were dried over anhydrous magnesium sulfate. The ethyl acetate was removed by distillation in vacuo with displacement by toluene to a final volume of 150 ml. The resulting slurry was heated to reflux (solution), cooled to 0°C., and filtered to 35 yield 5-(3-thienyl)oxazolidine-2,4-dione (8.92 g., 76.5%, m.p. 135-138°C.).
EXAMPLE 96
Sodium 5-(3-Thienyl)oxazolidine-2,4-dione 5-(3-Thienyl)oxazolidine-2,4-dione (3.0 g., 16.4 mmole) was dissolved in 60 ml. of ethyl acetate 5 and treated with 300 mg. of activated carbon. After stirring at 20°C. for 10 minutes, the mixture was filtered with ethyl acetate wash. Methanolic sodium hydroxide (3.78N, 4.2 ml.) was added and the sodium salt was allowed to crystallize. After about 30 minutes, 10 0.3 ml. of water was added. The slurry was granulated for 30 minutes at room temperature, then cooled to 5°C. and granulated for an additional 30 minutes. Filtration gave sodium 5-(3-thienyl)oxazolidine-2,4-dione as the monohydrate (3.37 g., 95%, m.p. 208-210°C.). 15 Analysis; Calcd. for C^H^O^NSNa.f^O:
C, 37.67; H, 2.71; N, 6.28; 0, 28.67; S, 14.37;
Na, 10.30; H20, 8.07.
Found: C, 37.35; H, 3.03; N, 6.24; O, 27.83; S, 14.33;
Na, 10.76; H20, 8.30.
Sodium hydroxide is substituted with an equivalent of potassium hydroxide, diethanolamine, meglumine or piperazine to produce the corresponding salts. The solvent is removed by evaporation or a non-solvent such as ether or hexane is added as necessary to 25 facilitate precipitation of the product.
The same methods are employed to produce the pharmaceutically acceptable salts of the other oxazolidine-2 , 4-diones of the present invention.
EXAMPLE 97
2-(3-Bromo-2-thienyl)-2-trimethylsiloxyethanenitrile 3-Bromo-2-thenaldehyde (6 g., 31 mmoles) and zinc 5 iodide (50 mg.) were combined with 180 ml. of methylene chloride. Trimethylsilylcarbonitrile (4.0 g., 5.2 ml., 41 mmoles) were added dropwise. The reaction mixture was stirred for 24 hours at room temperature, diluted with 50 ml. of methylene chloride, washed with 60 ml.
of 5% sodium bicarbonate and then with 50 ml. of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 2-(3-bromo-2-thienyl)-2-trimethylsiloxyethanenitrile (7.2 g., oil, m/e 291/289).
EXAMPLE 98
Ethyl l-(3-Bromo-2-thienyl)-l-
hydroxymethanecarboximidate Hydrochloride At 0°C., 2-(3-bromo-2-thienyl)-2-trimethylsiloxyethanenitrile (7.0 g., 24 moles) was dissolved in 210 ml. of ethanol saturated at 0°C. with hydrogen
chloride. After stirring for 30 minutes at the same temperature, the reaction mixture was evaporated to dryness. Trituration of the solid residue with ether afforded ethyl 1-(3-bromo-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride (7.0 g., m.p. 120-122°C.).
//' -97-
EXAMPLE 9 9
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-(3-Bromo-2-thienyj)oxazolidine-2, 4-dione Ethyl 1-(2-bromo-2-thienyl)-1-hydroxymethanecarboximidate hydrochloride (6.8 g., 23 mmoles) and 5 triethylamine (7.6 g., 10.5 ml., 76 mmoles) were combined in 250 ml. of tetrahydrofuran. The mixture was cooled to 0-5°C., perfused with phosgene for 30 minutes, warmed to room temperature, stirred for 16 hours, and poured slowly into 300 ml. of crushed ice. The quenched reaction mixture was extracted 10 twice with 200 ml. portions of chloroform. The combined chloroform extracts were washed with 60 ml. of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to an oil. Addition of hexane and ether afforded crystalline product. Recrystalliza-15 tion from toluene gave 5-(3-bromo-2-thienyl)oxazolidine-2,4-dione (2.25 g.; m.p. 138-139°C.).
Analysis: Calcd. for C7H4C>3NSBr:
C, 32.09; H, 1.59; N, 5.34; S, 12.21.
Found: C, 32.41; H, 1.75; N, 5.49; S, 12.61.
-98-EXAMPLE 100
-(5-Bromo-2-thienyl)-2-thioxooxazolidin-4-one Potassium cyanide (7.9 g., 0.123 mole) and potassium thiocyanate (10 g.f 0.104 mole) were combined in 8.5 ml. of water and stirred at 0°C. 5-Bromo-2-thenaldehyde (20 g., 0.104 mole) was added, yielding a slurry. Hydrochloric acid (30%, 50.7 ml.) was added, producing an oil ball. The reaction mixture was diluted with 104 ml. of water and stirred for 48 hours, by which time a granular solid had formed. Solids were recovered by filtration and distributed between chloroform and 5% sodium bicarbonate. The mixture was filtered, and the aqueous layer separated, acidified and the precipitated product recovered by filtration. Recrystallization from toluene gave purified 5-(5-bromo-2-thienyl)-2-thioxooxazolidin-4-one (2.08 g., m.p. 119-120 °C., m/e 279/277).
Analysis: Calcd. for C^H4BrN02S2:
C, 30.23; H, 1.95; N, 5.04.
Found: C, 30.54; H, 1.72; N, 5.26.
97
EXAMPLE 101 5-(5-Bromo-2-thienyl)oxazolidine-2,4-dione 5-(5-Bromo-2-thienyl)-2-thioxooxazolidin-4-one (1.5 g.) was dissolved in 1:1 water:ethanol (10 ml.) at 50°C. Hydrogen peroxide (30%, 7.0 ml.) was added to the stirred solution, which became somewhat turbid. Turbidity was reduced by the addition of 1 ml. of ethanol. The mixture was heated at 70°C. for 30 minutes, cooled somewhat, diluted with 100 ml. water and extracted with chloroform. The chloroform extract was washed with two 50 ml. volumes of sodium bicarbonate. The combined aqueous extracts were clarified by filtration, acidified with hydrochloric acid to pH 1.0, and filtered to yield 5-(5-bromo-2-thienyl)oxazolidine-2,4-dione (0.51 g., 36%; m.p. 139-139.5°C.; m/e 263/261).
Analysis: Calcd. for C7H4BrN03S:
C, 32.08; H, 1.54; N, 5.34.
Found: C, 32.16; H, 1.69; N, 5.47.
EXAMPLE 102 5-Hydroxy-5-(3-methoxy-2-thienyl)-2,4,6(1H,3H,5H)-pyrimidinetrione 3-Methoxythiophene [2.4 g., crude material prepared according to Arkiv. Kemi. 12, 239-246 (1958); Chem.
Abstr. 52, 20115d] and alloxan hydrate (3.2 g.) were dissolved by heating in 25 ml. of ethanol. Hydrochloric acid (IN, 3 ml., 3 mmoles) was added and the mixture refluxed for 3 minutes. The mixture was cooled to room temperature and diluted with 15 ml. of water to induce further crystallization of product. Filtration with 1:1 ethanol:water and then water wash gave 5-hydroxy-5-(3-methoxy-2-thienyl)2,4,6(1H,3H,5H)-pyrimidine trione [1.5 g., m.p. 190-210°C. (dec.); R^ 0.3 (1:1 hexane:ethyl acetate with 5% acetic acid); m/e 256].
78 5
EXAMPLE 103
-(3-Methoxy-2-thienyl)oxazolidine-2,4-dione 5-Hydroxy-5-(3-methoxy-2-thienyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (1 g.) was dissolved in IN sodium 5 hydroxide (20 ml.) and stirred for 1 hour. The mixture was acidified, clarified, extracted twice with 50 ml. portions of ethyl acetate. The combined ethyl acetate extracts were back-washed with water and evaporated to dryness (0.5 g. of solids). Chromatography on about 10 85 ml. of silica gel, monitored by tic, afforded 5-(3-
methoxy-2-thienyl)oxazolidine-2,4-dione (300 mg., m.p. 156-158°C.).
Analysis: Calcd. for Cgl^O^NS:
C, 45.08; H, 3.31; N, 6.57.
Found: C, 45.21; H, 3.39; N, 6.47.
EXAMPLE 104 5-Hydroxy-5-(5-phenyl-2-furyl)-2,4,6(1H,3H,5H)-pyrimidinetrione 2-Phenylfuran (5.76 g., 40 mmoles) was combined 20 with 100 ml. of tetrahydrofuran and cooled to -30°C.
Butyl lithium in hexane (2.3M, 19.1 ml.) was added dropwise over 5 minutes, keeping the temperature between -20° and -30°C. The reaction mixture was allowed to warm to room temperature and then recooled 25 to -30°C. Sublimed alloxan (5.96 g., 42 mmoles) in
40 ml. of tetrahydrofuran was added over 5 minutes, again keeping the temperature -20° to -30°C. The reaction mixture was again allowed to warm to room temperature, then recooled to 0°C. and 50 ml. of IN 30 hydrochloric acid added portionwise over 2-3 minutes. The quenched reaction mixture was extracted with 100 ml. of ethyl acetate. The extract was filtered through a bed of anhydrous magnesium sulfate, and evaporated to yield 5-hydroxy-5-(5-phenyl-2-furyl)-35 2,4,6(1H,3H,5H)pyrimidinetrione [9.4 g., gummy solid,
0.75 (1:1 hexane ethyl acetate/5% acetic acid)] contaminated with starting material (R^ 0.45).
EXAMPLE 105 5-(5-Phenyl-2-furyl)oxazolidine-2,4-dione 5 5-Hydroxy-5-(5-phenyl-2-furyl)-2,4,6(1H,3H,5H)-
pyrimidinetrione (0.7 g.) was dissolved in 15 ml. of IN sodium hydroxide, stirred at room temperature for 15 minutes, extracted with ethyl acetate, made slightly acidic with about 1 ml. of glacial acetic acid, and 10 extracted with 25 ml. of ethyl acetate. The latter ethyl acetate extract was back washed with about 6.5 ml. of water, filtered over a bed of anhydrous magnesium sulfate and evaporated to yield solid 5—(5— phenyl-2-furyl)oxazolidine-2,4-dione [100 mg.; m.p. 15 216-218°C.; R^ 0.6 (1:1 hexane:ethyl acetate/5% acetic acid)].
EXAMPLE 106 5-Hydroxy-5-(5-methyl-2-furyl)-2,4,6(1H,3H,5H)pyrimidinetrione 20 2-Methylfuran (3.28 g., 3.58 ml., 40 mmoles) was combined with 100 ml. of tetrahydrofuran. The reaction mixture, flushed with nitrogen, was cooled to -30°C. and butyl lithium (19.1 ml. of 2.3M in hexane) was added over a period of 10 minutes, maintaining the 25 temperature at -20 to -30°C. The reaction mixture was warmed to room temperature and then back to -30°C. Sublimed alloxan (5.96 g.) in 40 ml. of tetrahydrofuran was added dropwise over 10 minutes, keeping the temperature at -20 to -30°C. The reaction mixture was 30 warmed to room temperature, cooled to 0°C. and 50 ml.
of IN hydrochloric acid added portionwise, keeping the temperature at 0 to 5°C. The reaction mixture was extracted with 100 ml. of ethyl acetate. The extract was back washed with 25 ml. of water, filtered through
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a bed of anhydrous magnesium sulfate and evaporated to yield solid 5-hydroxy-5-(5-methyl-2-furyl)-2,4,6(1H,3H,5H) pyrimidinetrione (6.3 g.; m/e 224).
EXAMPLE 107 5-(5-Methyl-2-furyl)oxazolidine-2,4-dione 5-Hydroxy-5-(5-methyl-2-furyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (6.3 g.) was dissolved in 50 ml. of IN sodium hydroxide and stirred at room temperature for 15 minutes. The reaction mixture was extracted with 50 ml. of ethyl acetate, and acidified with glacial acetic acid. Product was then extracted into fresh ethyl acetate (three 30 ml. portions). The combined ethyl acetate extracts were filtered through a bed of anhydrous magnesium sulfate and evaporated to an oil. The oil was chromatographed on 50 ml. of silica gel, with 1:1 hexane:ethyl acetate/5% acetic acid as eluant. The column was monitored by tic using the same eluant. Clean product containing fractions were combined, evaporated to dryness and triturated 20 with hexane (311 mg., m.p. 135-138°C.). Recrystalliza-
tion from methanol/water afforded purified 5-(5-methyl-2-furyl)oxazolidine-2,4-dione (142 mg., m.p. 136.5-137.5°C.).
Analysis: Calcd. for CgH^NO^:
C, 53.04; H, 3.90; N, 7.73.
Found: C, 52.82; H, 4.03; N, 7.65.
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EXAMPLE 108 5-Hydroxy-5-(3-thienyl)-2,4, 6(1H,3H,5H)pyrimidinetrione Isopropyl ether (40 ml.) was cooled to -70°C.
Butyl lithium in hexane (2.4M, 10 ml., 24 mmoles) was added over 10 minutes, keeping the temperature -70° to -60°C. 3-Bromothiophene (1.9 ml., 20 mmoles) was added over 20 minutes, keeping the temperature -72° to -68°C. The mixture was stirred for an additional 10 30 minutes at -72° to -70°C. Sublimed alloxan (3 g., 21 mmoles) in 25 ml. of tetrahydrofuran was added over 4 0 minutes, keeping the temperature -70° to -65°C.
Stirring at this temperature was continued for 15 minutes. The cooling bath was removed and the reaction mixture 15 stirred for one hour at room temperature, then cooled to 5°C. Hydrochloric acid (IN, 40 ml.) was added slowly, and the organic phase separated. The aqueous phase was extracted with 3 5 ml. of ethyl acetate. The combined organic phase/extract was washed with 10 ml. 20 of water, dried over anhydrous sodium sulfate and concentrated to yield solid 5-hydroxy-5-(3-thienyl)-2,4,6(1H,3H,5H)pyrimidinetrione (1.41 g., 31%; m/e 226).
When this reaction was carried out in tetrahydro-25 furan with reverse addition of the 3-bromothiophene to butyl lithium, with immediate addition of 0.5 equivalent of alloxan hydrate in place of 1 equivalent of anhydrous alloxan, the product was a mixture of the above trione and 5-(3-bromo-2-thienyl)-5-hydroxy-2,4,6(1H,3H,5H)-30 pyrimidinetrione, which in turn was converted to a mixture of 5-(3-bromo-2-thienyl)oxazolidine-2,4-dione and 5-(3-thienyl)oxazolidine-2,4-dione by the method of Example 55.
EXAMPLE 109
-(3-Thienyl)oxazolidine-2,4-dione 5-Hydroxy-5-(3-thienyl)-2,4,6(1H,3H,5H)pyrimidinetrione (1.16 g., 5.1 mmoles) was dissolved in IN 5 sodium hydroxide (11 ml., 11 mmoles) and allowed to stand at room temperature for 15 minutes. The solution was acidified with acetic acid, and product allowed to crystallize over 35 minutes. Filtration gave 5-(3-thienyl)oxazolidine-2,4-dione (480 mg., 51%; m.p. 10 133-135°C.). An additional crop of product was obtained by extracting the mother liquor with ethyl acetate. The extract was back washed with water, and evaporated to dryness (80 mg., contaminated with starting material).
EXAMPLE 110
-(3-Furyl)-5-hydroxy-2,4,6(1H,3H,5H)pyrimidinetrione The detailed procedure of Example 108, but substituting 3-bromofuran (2.94 g., 1.8 ml., 20 mmoles) for the 20 3-bromothiophene, was employed to produce 5-(3-furyl)-5-hydroxy-2,4,6(1H,3H,5H)pyrimidinetrione (1.62 g., oil, m/e 210).
EXAMPLE 111 5-(3-Furyl)oxazolidine-2,4-dione 25 5-(3-Furyl)-5-hydroxy-2,4,6(1H,3H,5H)pyrimidine trione (1.62 g.) was dissolved in 15 ml. of IN sodium hydroxide, and allowed to stand for 15 minutes at room temperature, and then extracted with 5 ml. of ethyl acetate. The aqueous layer was acidified with glacial 30 acetic acid (about 1.5 ml.) and product extracted into 25 ml. of ethyl acetate. The extract was back washed with 5 ml. of water, filtered through a bed of anhydrous sodium sulfate, and evaporated to yield crude product as an oil (470 mg., m/e 167). Crystallization from 35 chloroform gave purified 5-(3-furyl)oxazolidine-2,4-dione (129 mg., m.p. 88-90°C., m/e 167). A second,
lower melting crop was obtained from mother liquor.
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EXAMPLE 112
3-Thenaldehyde Cyanohydrin Sodium bisulfite (30.2 g., 0.29 mole) was dissolved in 190 ml. of water and warmed to 50°C. 3-Thenaldehyde 5 (25 g., 0.22 mole) was added and the reaction mixture held at 50-55°C. for 35 minutes, by which time all but a small amount of gummy solids were in solution. The mixture was cooled to 5°C. and layered with 190 ml. of isopropyl ether. With stirring, sodium cyanide 10 (24.8 g., 0.25 mole) in 190 ml. of water was added dropwise over 20 minutes, keeping the temperature below 10°C. Stirring was continued at room temperature for 1 hour. The organic layer was separated, and the aqueous phase extracted with fresh isopropyl ether 15 (300 ml.). The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to yield 3-thenaldehyde cyanohydrin as an oil (28.3 g., 92%).
EXAMPLE 113
2-Hydroxy-2-(3-thienyl)acetamide
Formic acid (0.5 ml.) was cooled in an ice-water bath. 3-Thenaldehyde cyanohydrin (1.0 g.) and then concentrated hydrochloric acid (0.5 ml.) were added. The reaction mixture was stirred at room temperature 25 for 1 hour, poured over crushed ice, and extracted with three portions of ethyl acetate. The combined extracts were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to an oil, which partially crystallized on scratching. 30 Recrystallization from ethyl acetate gave 2-hydroxy-2-
(3-thienyl)acetamide (389 mg., 35%, m.p. 123-126°C., m/e 157).
EXAMPLE 114 Mixed Methyl/Ethyl Esters of 2-Benzoyl-2-(3-thienyl)malonic Acid Commercially available mixed esters of 2-(3-5 thienyl)malonic acid (47% diethyl, 43% methyl/ethyl, 10% dimethyl; 11.4 g.) were added portionwise to a dispersion of sodium hydride in oil (50%, 2.4 g.) slurried in 70 ml. of toluene. An exotherm was noted, the temperature rising to 45°C. The reaction mixture 10 was stirred for 3 hours at room temperature, and then cooled in an ice-water bath. Benzoyl peroxide (8 g.) in 100 ml. of toluene was added over a period of 1 hour, maintaining the temperature 10-20°C. The mixture was stirred for 30 minutes at room temperature, 15 diluted dropwise with 50 ml. of water (initial foaming noted), and finally diluted with 50 ml. of ether. The organic phase was separated, back washed with three 25 ml. portions of water, and evaporated to yield mixed methyl/ethyl esters of 2-benzoyloxy-2-(3-thienyl)-20 malonic acid as an oil (15.5 g. containing about
1.2 g. of oil from the sodium hydride dispersion).
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EXAMPLE 115 5-(3-Thienyl)oxazolidine-2,4-dione Sodium (0.46 g., 20 mmoles) was dissolved in 50 ml. of absolute ethanol. To the resulting warm 5 solution of sodium ethoxide (about 60°C.), crude mixed esters of 2-benzoyloxy-2-(3-thienyl)malonic acid (7 g., approximately 20 mmoles, as prepared in Example 60) were added, followed by urea (1.2 g., 20 mmoles)
dissolved in 20 ml. of hot ethanol. The reaction 10 mixture was heated in an oil bath at 105-110°C. for
4.5 hours. The reaction mixture was cooled, acidified with concentrated hydrochloric acid, and extracted with ethyl acetate. The extract was back washed with water and concentrated to an oil. Trituration with 15 2 0 ml. of 1:1 ether:hexane gave a mixture of 5-(3-
thienyl)oxazolidine-2,4-dione and intermediate 5-benzoyloxy-5-(3-thienyl)2,4,6(1H,3H,5H)pyrimidinetrione (0.8 g.). A portion of this mixture (0.3 g.) was dissolved in IN sodium hydroxide (5 ml.) and allowed 20 to stand for 20 minutes at room temperature. The reaction mixture was clarified by filtration, and acidified with acetic acid to precipitate 5-(3-thienyl)-oxazolidine-2,4-dione (100 mg., m.p. 136-138°C.).
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EXAMPLE 116 2-(3-Benzo[b]thienyl)-2-trimethylsiloxyethanenitrile Benzo[b]thiophene-3-carbaldehyde [1.8 g., 11 mmoles, J. Chem. Soc. C., pp. 339-340 (1969)] and about 100 mg. of zinc iodide were combined in 35 ml. of ether. Trimethylsilylcarbonitrile (1.98 g., 20 mmoles) was added dropwise. After approximately 1 hour, the reaction mixture was washed in sequence with saturated sodium bicarbonate, water and brine, dried over anhydrous sodium sulfate, filtered and evaporated to yield 2-(3-benzo[b]thienyl)-2-trimethylsiloxyethane-nitrile [2.5 g., oil, 0.7 (1:2 ethyl acetate:hexane)].
EXAMPLE 117 Ethyl 1-(3-Benzo[b]thienyl)-1-hydroxymethanecarboximidate Hydrochloride With cooling in an ice-water bath, 2-(3-benzo[b]-thienyl)-2-trimethylsiloxyethanenitrile (2.3 g.) was dissolved in 10 ml. of saturated ethanolic hydrogen chloride, and held for 16 hours at about 5°C. The reaction mixture was evaporated to dryness and triturated with ether to yield 1-(3-benzo[b]thienyl)-1-hydroxymethanecarboximidate hydrochloride (2.2 g., m.p. 128-131°C., m/e 235).
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EXAMPLE 118 5-(3-Benzo[b]thienyl)oxazolidine-2,4-dione Ethyl 1-(3-benzo[b]thienyl)-1-hydroxymethanecarboximidate hydrochloride (2.36 g., 8.7 mmoles) and 5 triethylamine (2.64 g., 26 mmoles) were combined in
0 ml. of tetrahydrofuran and cooled to 10°C. Phosgene was bubbled through the cooled reaction mixture for 3 0 minutes, followed by a 10 minute flush with nitrogen. The reaction mixture was slowly poured into 100 ml. of 10 ice and extracted twice with ether. The combined ether extracts were back-washed with water and then brine, dried over anhydrous sodium sulfate, filtered, and evaporated to yield a gummy solid (1.7 g.). This crude product was dissolved in IN sodium hydroxide, 15 washed twice with ether and acidified with 6N hydrochloric acid, affording purified 5-(3-benzo[b]thienyl)-oxazolidine-2,4-dione (950 mg., m.p. 202-205°G., m/e 233) .
Analysis; Calcd. for C^^H^O^NS:
C, 56.64; H, 3.02; N, 6.00.
Found: C, 56.74; H, 3.18; N, 5.69.
EXAMPLE 119 2-(7-Benzo[b]thienyl)-2-trimethy1s iloxyethanenitrile 25 Benzo[b]thiophene-7-carbaldehyde [1.3 g., 8 mmoles,
J. Org. Chem. 39, 2829 (1974)] was dissolved in 35 ml. of ether. Trimethylsilylcarbonitrile (1.5 ml., 12 mmoles) and zinc iodide (about 50 mg.) were added and the mixture stirred for 1 hour at room temperature, 30 at which time tic indicated conversion was complete.
The reaction mixture was evaporated to dryness, yielding 2-(7-benzo[b]thienyl)-2-trimethylsiloxyethanenitrile [2.2 g., oil; 0.6 (1:5 ethyl acetate:hexane/5%
acetic acid)].
EXAMPLE 120
Ethyl 1-(7-Benzo[b]thienyl)-1-hydroxymethanecarboximidate Hydrochloride By the procedure of Example 112, 2-(7-benzo[b]-5 thienyl)-2-trimethylsiloxyethanenitrile (2.1 g.),
using 35 ml. of saturated ethanolic hydrogen chloride, was converted to ethyl 1-(7-benzo[b]thienyl-l-hydroxy-methanecarboximidate hydrochloride (1.1 g., m.p. 120-122°C.), after crystallization from acetone. 10 EXAMPLE 121
-(7-Benzo[b]thienyl)oxazolidine-2,4-dione Following the procedure of Example 118, ethyl 1-(7-benzo[b]thienyl)-1-hydroxymethanecarboximidate hydrochloride (1.1 g., 4 mmoles) and triethylamine 15 (1.7 ml., 12 mmoles) were reacted with phosgene. The crude product, isolated as an oil, was dissolved in 25 ml. ether and product extracted into 50 ml. of IN sodium hydroxide. This aqueous extract was acidified with concentrated hydrochloric acid and product 20 extracted into fresh ether, which was back washed with water and evaporated in vacuo to a solid residue (670 mg.). This residue was recrystallized to yield 5-(7-benzo[b]thienyl)oxazolidine-2,4-dione (0.45 g., m.p. 130-132°C.).
Analysis: Calcd. for C^H^^NS:
C, 56.64; H, 3.02; N, 6.00.
Found: C, 56.42; H, 3.18; N, 5.91.
EXAMPLE 122 5-Hydroxy-5-(5-methoxy-2-thienyl)-2,4,6(1H,3H,5H)-pyrimidinetrione 2-Methoxythiophene (2.3 g., 20 mmoles) was dis-5 solved in 35 ml. of ether. With cooling, butyl lithium in hexane (2.4M, 9 ml., 21.6 mmoles) was added dropwise over 15 minutes, the temperature rising as high as 35°C. during this addition. The reaction mixture was stirred for 1 hour at room temperature. 10 While maintaining the temperature between -20° and -15°C., sublimed alloxan (3 g., 21 mmoles) in 20 ml. of tetrahydrofuran was added during 10 minutes. The mixture was warmed to room temperature, stirred for 0.5 hour, cooled to 5°C. and quenched by adding 35 ml. 15 of IN hydrochloric acid in portions. The organic phase was separated and the aqueous phase extracted with 25 ml. of ethyl acetate. The combined organic phase and extract were back-washed with water, concentrated to dryness and triturated with hexane to yield 20 solid 5-hydroxy-5-(5-methoxy-2-thienyl)-2,4,6(1H,3H,5H)-pyrimidinetrione (1.4 g., m/e 256).
EXAMPLE 123
-(5-Methoxy-2-thienyl)oxazolidine-2,4-dione 5-Hydroxy-5-(5-methoxy-2-thienyl)-2,4,6(1H,3H,5H)-25 pyrimidinetrione (1.1 g.) was dissolved in 10 ml. of IN sodium hydroxide, allowed to stand for 1.5 hours at room temperature, extracted with ether, acidified with acetic acid, diluted with 15 ml. of water and filtered to yield product [567 mg., m.p. 144-146°C. (dec.)]. 30 Recrystallization from acetone-hexane gave purified 5-(5-methoxy-2-thienyl)oxazolidine-2,4-dione in two crops [487 mg., m.p. 147-148°C. (dec.)].
Analysis; Calcd. for CgH^O^NS:
C, 45.08; H, 3.31; N, 6.57.
Found: C, 45.08; H, 3.41; N, 6.39.
1
4
EXAMPLE 124 5-[5-(2-phenyl-l,3-dioxolan-2-yl)-2-thieny 1 ]-2,4 , 6 (1H, 3H, 5H) -pyrimidinetrione At room temperature, 2-phenyl-2-thienyl)-1,3-dioxolane (3.26 g., 14 mmoles) was dissolved in 35 ml. of ether. Butyl lithium in hexane (2.4M, 6.25 ml., 15 mmoles) was added dropwise over 15 minutes, the temperature rising to 33°C. The mixture was stirred for 75 minutes at room temperature and then cooled. Maintaining the temperature between -15° and -20°C., sublimed alloxan (2.13 g., 15 mmoles) in 20 ml. of tetrahydrofuran was added dropwise over 10 minutes. The reaction mixture was stirred at room temperature for 30 minutes, cooled to 5°C., quenched with 35 ml.
of IN hydrochloric acid, added in small portions, and extracted with 25 ml. of ethyl acetate. The organic layer was back washed with 15 ml. of water, filtered through a bed of anhydrous sodium sulfate, and evaporated to yield 5-[5-(2-phenyl-l,3-dioxolan-2-yl)thienyl]-2,4,6(1H,3H,5H)-pyrimidinetrione [oil, 0.25 (1:1 hexane:ethyl acetate/5% acetic acid)] contaminated
0.8) .
EXAMPLE 125
with starting material (R^ 0.8).
-[5-(2-Phenyl-l,3-dioxolan-2-yl)-2-
thienyl]oxazolidine-2,4-dione
The entire crude product from the preceding Example was taken into 35 ml. of IN sodium hydroxide and allowed to stand for 30 minutes. After acidification the product was extracted into isopropyl ether. The extract was back washed with water and evaporated to yield 5-[5-(2-phenyl-l,3-dioxolan-2-yl)thienyl]-oxazolidine-2,4-dione [0.40 g., R^ 0.65 (1:1 ethyl acetate:hexane/5% acetic acid)].
EXAMPLE 126
-(5-Benzoyl-2-thienyl)oxazolidine-2,4-dione 5-[5-(2-Phenyl-l,3-dioxolan-2-yl)-2-thienyl]-oxazolidine-2,4-dione (0.40 g.) was dissolved in 30 ml. of ether and stirred with 10 ml. of 6N hydrochloric acid at room temperature for 1 hour. Ethyl acetate (10 ml.) was added, and the organic layer was separated and evaporated in vacuo to dryness (0.388 g.) Chromatography on 50 ml. of silica gel, eluted with 1:1 hexane:ethyl acetate/5% acetic acid and monitored by tic, gave in early fractions purified 5-(5-benzoyl-2-thienyl)oxazolidine-2,4-dione (0.22 g., m.p. 153-155° m/e 287).
Analysis: Calcd. for C^HgO^NS:
C, 58.52; H, 3.16; N, 4.87.
Found: C, 58.69; H, 3.50; N, 4.94.
EXAMPLE 127 5-(3-Thienyl)oxazolidine-2,4-dione Capsules The following ingredients were combined and blended for 30 minutes:
Sodium 5-(3-thienyl)oxazolidine-2,4-dione monohydrate 30.46
Lactose, anhydrous, U.S.P. 14.05
Corn starch, dried, U.S.P. 5.00
♦Equivalent to 25 g. of active drug (unsolvated free acid).
The mixture was milled (0.040 inch plate) and blended for an additional 30 minutes. Magnesium ' stearate, sodium lauryl sulfate, 90/10 blend (1.00 g.) was added and the mixture blended for 20 minutes. The blend was filled into #0 gelatin capsules (505 mg.
fill weight) so as to obtain capsules of 250 mg. potency.
//'
Larger capsules are employed to prepare capsules of higher potency.
The same procedure was employed to prepare capsules of 100 mg. potency from the following ingre-5 dients:
Sodium 5-(3-thienyl)oxazolidine-2,4-dione monohydrate 12.18 g,
Lactose, anhydrous, U.S.P. 32.32 g,
Corn starch, dried, U.S.P. 5.00 g,
Magnesium stearate/lauryl sulfate
(90/10 blend) 0.50 g,
♦Equivalent to 10 g. of activated ingredient
(unsolvated free acid).
A lower level of active ingredient in the blend 15 is used to prepare capsules of lower potency.
EXAMPLE 128 Tablets
A tablet base is prepared by blending the following ingredients in the proportion by weight indicated: 20 Sucrose, U.S.P. 80.3
Tapioca starch 13.2
Magnesium stearate 6.5
Into this tablet base there is blended sufficient sodium 5-(3-thienyl)oxazolidine-2,4-dione monohydrate 25 to form tablets containing 50 mg., 100 mg. or 250 mg.
of active drug (weight equivalent to the free acid). The portion of blend to active drug is within the limits of 1-0.167 to 1-1, e.g., in the extremes, 60.2 mg. of sodium salt monohydrate and 300 mg. of 30 blend in a 50 mg. tablet or 304.6 mg. of sodium salt monohydrate and 250 mg. of blend in a 250 mg. tablet.
EXAMPLE 129
Injectable Preparation Sterile sodium 5-(3-thienyl)oxazolidine-2,4-dione is dry filled into vials so as to contain 670.1 mg. of 5 the sodium salt monohydrate per vial (equivalent to 550 mg. of free acid). Prior to use, sterile water for injection (11 ml.) is added, and the mixture shaken to form a solution, containing 50 mg./ml. of active drug, which is suitable for intravenous, intra-10 muscular or subcutaneous injection.
Alternatively vials are filled by a freeze drying procedure. Two ml. of a sterile, aqueous solution containing 335 mg./ml. of sodium salt monohydrate is introduced into each vial. The vials are freeze dried 15 on trays.
EXAMPLE 130 3-Ethoxycarbonyl-5-(3-thienyl)oxazolidine-2,4-dione Sodium 5-(3-thienyl)oxazolidine-2,4-dione mono-20 hydrate is stripped of water by drying in vacuo at elevated temperature (50-70°C.). The anhydrous salt (2.05 g., 10 mmoles) is suspended in 35 ml. of 1,2-dichloroethane. Ethyl chloroformate (1.41 g., 10 mmoles) is added and the mixture refluxed for about 2 hours. 25 The reaction mixture is cooled to room temperature, byproduct sodium chloride removed by filtration and the filtrate concentrated to dryness to yield 3-ethoxy-carbonyl-5-(3-thienyl)oxazolidin-2,4-dione.
Substitution of the ethyl chloroformate with an 30 equivalent quantity of acetyl chloride, isobutyryl chloride, N,N-dimethylcarbamoyl chloride, or benzoyl chloride produces, respectively, 3-acetyl-5-(3-thienyl)-oxazolidine-2,4-dione, 3-isobutyroyl-5-(3-thienyl)-oxazolidine-2,4-dione, 3-(N,N-dimethylcarbamoyl)-5-(3-35 thienyl)oxazolidine-2,4-dione and 3-benzoyl-5-(3-thienyl)oxazolidine-2,4-dione.
1 97
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EXAMPLE 131 3-Acetyl-5-(3-thienyl)oxazolidine-2,4-dione
Method A
-(3-Thienyl)oxazolidine-2,4-dione (1.83 g., 5 10 mmoles) and triethylamine (0.14 ml., 10 mmoles) are combined with 25 ml. of 1,2-dichloroethane at room temperature. Acetyl chloride (0.72 ml., 10 mmoles) is added dropwise over a few minutes and the reaction mixture stirred for 3 hours. The reaction mixture is 10 evaporated to dryness and the residue distributed between saturated sodium bicarbonate and chloroform. The chloroform layer is washed with water, and then brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield 3-acetyl-5-(3-thienyl)-15 oxazolidine-2,4-dione.
Method B
-(3-Thienyl)oxazolidine-2,4-dione (1.83 g., 10 mmoles) and acetic anhydride (1.14 ml., 12 mmoles) are combined with 20 ml. of tetrahydrofuran and 20 stirred for 40 hours. The reaction mixture is evaporated to dryness and 3-acetyl-5-(3-thienyl)oxazolidine-2,4-dione further isolated as in Method A.
The same procedure, but substituting acetic anhydride with an equivalent of acetoformic acid 25 reagent [a solution of acetic-formic anhydride in acetic acid; cjf. Blackwood et al_., J. Am. Chem. Soc., 82, 5194 (I960)], propionic anhydride or benzoic anhydride, allows formation of corresponding 3-formyl-5-(3-thienyl)oxazolidine-2,4-dione, 3-propionyl-5-(3-30 thienyl)oxazolidine-2,4-dione and 3-benzoyl-5-(3-
thienyl)oxazolidine-2,4-dione.
EXAMPLE 132 3-(N-Methylcarbamoyl)-5-(3-thienyl)oxazolidine-2,4-dione 5-(3-Thienyl)oxazolidine-2,4-dione (1.83 g., 5 10 moles) and one drop of triethylamine are combined in 35 ml. of 1,2-dichloroethane. Methyl isocyanate (0.58 ml., 10 mmoles) is then added and the reaction mixture stirred for 4 hours at room temperature. The reaction is diluted with 35 ml. of 1,2-dichloroethane, 10 washed with saturated sodium bicarbonate and then brine, dried over magnesium sulfate, filtered and concentrated to yield 3-(N-methyl)-5-(3-thienyl)-oxazolidine-2,4-dione.
1 97
/ ^
EXAMPLE 133
3-(4-Methoxy-3-thienyl)-2-trimethylsiioxyethanenitrile By the procedure of Example 55, 4-methoxy-3-thenaldehyde (2.6 g., 18.3 mmole) and trimethylsilyl-5 carbonitrile (2.15 g., 21.7 mmole) in 250 ml. of ether in the presence of 50 mg. of zinc iodide was converted to title product as an oil (3.9 g., m/e 241).
EXAMPLE 134 Methyl 1-Hydroxy-l-(4-methoxy-3-thienyl) 10 methanecarboximidate Hydrochloride
Saturated methanolic hydrogen chloride (100 ml.) was maintained at 0-5°C. in an ice bath. Title product of the preceding Example (3.9 g.) in 20 ml. of methanol was added dropwise and the mixture held for 1 hour at 15 0-5°C. The reaction mixture was concentrated to solids and the residue triturated with ether to yield the title product [2.76 g., m.p. 94-99°C. (dec.)]. Recrystallization from methanol-ether gave purified title product [1.51 g.; m.p. 112-114 (dec.); m/e 201]. 20 EXAMPLE 135
-(4-Methoxy-3-thienyl)oxazolidine-2,4-dione By the procedure of Example 57, the product of the preceding Example (1.3 g., 5.5 mmoles) and triethylamine (1.7 g., 17 mmoles) in 50 ml. of tetrahydrofuran were 25 reacted with phosgene for 30 minutes at 0-5°C. The reaction mixture was stirred overnight at room temperature. The reaction mixture was poured slowly into 500 ml. of crushed ice and extracted with three 50 ml. portions of chloroform. The combined organic layers 30 were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to solids. Recrystallization from toluene gave purified title product [510 mg. m.p. 120-222°C.; ir (KBr) 1377, 1732, 1767, 1808 cm"1]. Analysis; Calcd. for CgH^C^NS:
C, 45.06; H, 3.31; N, 6.57.
Found: C, 45.31;,H, 3.41; N, 6.85.
197
® c 4
EXAMPLE 136
3- (4-Ethoxy-3-thienyl) -2-trimethylsiloxyethanenitrile By the procedure of Example 55, 4-ethoxy-3-then-aldehyde (8.1 g., 0.052 mole) and trimethysilylcarbo-5 nitrile (6.13 g., 0.062 mole) in 300 ml. of ether, in the presence of 50 mg. of zinc iodide, were converted to title product (13 g.) as a viscous oil; pnmr indicated absence of the aldehyde proton.
EXAMPLE 137
Ethyl l-Hydroxy-l-(4-ethoxy-3-thienyl)-
methanecarboximidate Hydrochloride Dsing ethanol in place of methanol, but otherwise the procedure of Example 134, product of the preceding Example (13 g.) was converted to title compound 15 [9.23 g., m.p. 126-128° (dec.)].
EXAMPLE 138 5-(4-Ethoxy-2-thienyl)oxazolidine-2,4-dione Dsing a phosgene perfusion time of 1 hour at 0-5°C. and a further reaction time of 1 hour at room 20 temperature, product of the preceding Example (9.2 g.)
was converted to title product. To isolate the product, the reaction was poured in 1.5 1. of crushed ice and extracted with three 200 ml. portions of chloroform. The organic layers were combined and extracted with 25 three 15 0 ml. portions of IN sodium hydroxide. The basic extracts were combined, back-washed with 200 ml. of fresh chloroform, reacidified with 3N hydrochloric acid and extracted with three 200 ml. portions of chloroform. The last three organic extracts were 30 combined, washed with brine, dried over magnesium sulfate, filtered, evaporated to solids, and the residue crystallized from toluene to yield title compound [4.06 g., m.p. 144-146°C., m/e 227; ir (KBr) 1822, 1737, 1568 cm"1].
Analysis: Calcd. for CgH^O^NS:
C, 47.57; H, 3.99; N, 6.17 Found: C, 47.18; H, 4.04; N, 6.06.
The chloroform back-wash was reextracted with three 5 150 ml. portions of fresh IN sodium hydroxide. These basic extracts were combined and additional product (980 mg., m.p. 144-146°C.) recovered in like manner.
EXAMPLE 139 2-[4-(n-Propoxy)-3-thienyl]-2-10 trimethy1s iloxyethanenitri1e
By the procedure of Example 55, 4-(n-propoxy)-3-thenaldehyde (3.1 g., 18 mmoles) and trimethylsilylcarbonitrile (2.28 g., 2.9 ml., 23 mmoles) in 250 ml. of ether, in the presence of 5 0 mg. of zinc iodide, 15 were converted to title product as an oil [4.6 g.; m/e
558 cm"1].
EXAMPLE 140
269; ir (CH2C12) 2936, 1558 cm"1].
Ethyl 1-Hydroxy-l-[4-(n-propoxy)-3-thienyl]methanecarboximidate Hydrochloride 20 Dsing a reaction time of 20 minutes after comple tion of the addition, the procedure of Example 137 was used to convert the product of the preceding Example (4.5 g.) into title product of the present Example [3.05 g., m.p. 127-129°C. (dec.)]. 25 EXAMPLE 141
-[4-(n-Propoxy)-3-thienyl— oxazolidine-2,4-dione By the procedure of Example 135, the product of the preceding Example (2.8 g., 0.01 mole) was converted 30 to toluene recrystallized 5-[4-(n-propoxy)-3-thienyl]-oxazolidine-2,4-dione [1.63 g.; m.p. 134-136°C.; m/e 241; ir (KBr) 1827, 1747, 1564 cm"1].
EXAMPLE 142 2-(4-Methoxy-2-methyl-3-thienyl)-2-trimethylsiloxyethanenitrile By the procedure of Example 55, 4-methoxy-2-methyl-3-thenaldehyde (5.2 g., 3 3.3 mmoles) and trimethylsilylcarbonitrile (3.96 g., 40 mmoles) in 350 ml. of ether, in the presence of 50 mg. of zinc iodide, were converted to title product, isolated as a viscous oil [7.3 g.; m/e 255; ir (CH CI.) 1575, 1204, 1075 cm"1].
EXAMPLE 143 Ethyl 1-Hydroxy-l-(4-methoxy-2-methyl-3-thienyl)methanecarboximidate Hydrochloride The procedure of Example 137 was applied to the product of the preceding Example (7.2 g.) to produce 5.8 g. of a mixture of title compound and the corresponding ethoxy ether (estimated by pnmr to be about 4 0% methyl ether and 6 0% ethyl ether; showing both m/e 243 and 229).
A portion of this mixture (2.5 g.) was taken into 100 ml. of methanol, cooled to 0-5°C., and perfused with hydrogen chloride for 1 hour. After 1 hour additional stirring at 0°C., the reaction mixture was evaporated to a viscous oil. Crystallization from ether gave title product [2.1 g.; m.p. 123-125°C. (dec.); m/e 229].
The corresponding methyl imidate ester of the title product is obtained by directly reacting the product of the preceding Example with methanolic hydrogen chloride according to the procedure of Example 134.
1978 5
EXAMPLE 144 Ethyl l-(Hydroxy)-l-(4-Ethoxy-2-methyl-3-thienyl)methanecarboximidate Hydrochloride A portion of the mixed methyl and ethyl ethers of 5 the preceding Example (2.5 g.) was taken into 100 ml. of ethanol and cooled to 0°C. The cold solution was perfused with hydrogen chloride for 1 hour, stirred for an additional hour at 0°C. and evaporated to an oil. The oil was crystallized by trituration with 10 ether. Repulping in ether gave title product [2.07 g., m.p. 105-107°C. (dec.); m/e 243].
EXAMPLE 145
-(4-Methoxy-2-methyl-3-thienyl)oxazolidine-2,4-dione Using a reaction time of 3.5 hours at room tempera-15 ture, but otherwise following the procedure of Example 57, the product of Example 143 (2.0 g., 7.5 mmoles) was converted to toluene recrystallized title product [0.52 g., m.p. 179-181°C.; m/e 227; ir (KBr) 1820, 1750, 1727, 1583 cm"1]. 20 EXAMPLE 14 6
-(4-Ethoxy-2-methyl-3-thienyl)oxazolidine-2,4-dione By the procedure of the preceding Example, the product of Example 144 (1.9 g.) was converted to title product [245 mg., m.p. 136-138°C.; m/e 241; ir (KBr) 25 1824, 1743 cm"1].
1978 5
EXAMPLE 147 5-Hydroxy-(2,5-Dimethyl-3-furyl)-2,4, 6(1H,3H,5H)pyrimidinetrione Isopropyl ether (35 ml.) was cooled to -68°C.
Butyl lithium (5 ml. of 2.1M in hexane, 10.5 mmoles)
was added, allowing the temperature to rise to -60°C. 2,5-Dimethyl-3-iodofuran [J. Am. Chem. Soc. 70, p. 739 (1948); 1.2 ml, 9 mmoles] was then added dropwise keeping the temperature between -65 and -68°C. After 10 stirring for 0.5 hour at -68°C., anhydrous alloxan
(1.5 g., 10.6 mmoles) dissolved in 15 ml. of tetrahydrofuran was added dropwise over 30 minutes, keeping the temperature -65 to -60°C. The stirred reaction mixture was warmed over 15 minutes to 0°C., IN hydro-15 chloric acid (25 ml.) was added and the organic phase separated. The aqueous phase was extracted with 20 ml. of ethyl acetate. The combined organic layers were washed with 10 ml. of water and evaporated to yield title product (1 g., 0.05 (1:5 ethyl acetate: 20 hexane/5% acetic acid)].
"1978
EXAMPLE 148
-(2,5-Dimethyl-3-furyl)oxazolidine-2,4-dlone Product of the preceding Example (1 g.) was taken into 10 ml. of IN sodium hydroxide and held for 15 minutes. The solution was extracted with 5 ml. of ethyl acetate, acidified with acetic acid and extracted with 25 ml. of ethyl acetate. The acidic extract was back-washed with 5 ml. of water and evaporated to solids (340 mg.), which were chromatographed on 50 ml. of silica gel, using 1:1 ethyl acetate:hexane as eluant and tic monitoring. Clean fractions were combined, evaporated to dryness and the residue recyrstallized from ether-hexane to yield purified title product [170 mg.; m.p. 144-145°; m/e 195; Rf 0.3 (1:5 ethyl acetate:hexane/5% acetic acid); 0.55 (1:1 ethyl acetate:hexane)].
Analysis: Calcd. for CgHgO^N:
C, 55.38; H, 4.65; N, 7.18 Found: C, 55.15; H, 4.76; N, 7.04.
EXAMPLE 149 5-Hydroxy-5-(4-iodo-3-furyl)-2,4,6(1H,3H,5H)pyrimidinetrione 3,4-Diiodofuran (0.96 g. , 3 mmoles) in 5 ml. of 5 ether was added slowly to a cold (-65°C.) solution of butyl lithium (2 ml. of 2.3M in hexane, 4.6 mmoles) in 15 ml. of ether. The mixture was stirred for 20 minutes at -65°C. Anhydrous alloxan (0.57 g., 4 mmoles) was dissolved in 10 ml. of tetrahydrofuran and added 10 slowly to the 4-iodo-3-furyl lithium solution at -65°C. After 10 minutes at the same temperature, the reaction mixture was warmed to 15°C., acidified with 15 ml. of IN hydrochloric acid and extracted with ether. The ether extract was back-washed with 10 ml. of water, 15 concentrated to dryness and the residue triturated with 2 ml. of hexane to yield title product [108 mg.; m/e 336; R^ 0.5 (1:1 ethyl acetate:hexane/5% acetic acid)] .
1 97 * 5
EXAMPLE 150 5-(4-Iodo-3-furyl)oxazolidine-2,4-dione Product of the preceding Example (100 mg.) was allowed to stand with 1 ml. of IN sodium hydroxide for 5 15 minutes at room temperature. The reaction mixture was acidified with acetic acid and extracted with 3 ml. of ethyl acetate. The organic extract was back-washed with 1 ml. of water and evaporated to a gum (63 mg.). Crude material (120 mg.) prepared in this 10 manner was chromatographed on 50 ml. of silica gel using 1:1 ethyl acetate:hexane as eluant and tic monitoring. The first fractions from the column were combined and evaporated to a gum (78 mg. which crystallized from chloroform to yield purified title product 15 (45 mg.; m.p. 140-144°C.).
Analysis: Calcd. for C^H^O^NI:
C, 28.69; H, 1.38; N, 4.78 Found: C, 28.37; H, 1.62; N, 4.74.
''! 9 T c r
-127-EXAMPLE 151
-(5-Chloro-7-benzo[b]furanyl]oxazolidine-2,4-dione Title product of Example 50 (100 rag., 0.39 mmole) was suspended in 6 ml. of chloroform and bis(trimethyl-5 silyl)trifluoroacetamide (100 mg., 0.104 ml., 0.39 mmole)
added in one portion. After stirring for 1 minute, N-bromosuccinimide (69 mg., 0.39 mmole) was added together with a trace (a single crystal) of benzoyl peroxide. The mixture was heated to reflux for 2 hours, cooled 10 to room temperature, filtered from insolubles and evaporated to semisolids under a stream of nitrogen. The residue was partitioned between IN sodium hydroxide and ethyl acetate. The aqueous layer was separated, washed with fresh ethyl acetate, acidified with IN 15 hydrochloric acid and extracted with three portions of chloroform. The chloroform extracts were combined,
dried over anhydrous magnesium sulfate, filtered, concentrated to an oil, and title product crystallized from toluene (44 mg.; m.p. 154-157°C.; m/e 251.253). 20 By the same method the fluoro analog of Example 50
is converted to 5-(5-fluoro-7-benzo[b]furanyl]oxazolidine-2,4-dione.
• •
!l9?es
PREPARATION 1 2-Ethoxy-3-pyridinecarboxylic Acid Sodium ethoxide was prepared by adding sodium (1.4 g. , 0.06 mole) portion wise, to 50 ml. of anhydrous ethanol. The solution was diluted with 20 ml. of ethanol and 4.5 g. of 2-chloropyridine-3-carboxylic was added. The reaction mixture was heated in a steel pressure vessel at 17 0°C. for 6 hours. The vessel was cooled and the contents evaporated to dryness in vacuo. The residue was taken up in 150 ml. of water and acidified to constant pH 4.5. The water solution was saturated with salt and extracted with four portions of ethyl acetate. The combined ethyl acetate layers were back washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product (4.33 g., m.p. 85-88°C.).
LI 973
PREPARATION 2 2-Methoxy-3-pyridinecarboxylic Acid A stainless steel stirred autoclave was charged sequentially with methanol (2.8 1.), sodium methoxide (259 g.) (in portions, keeping the temperature less than 35°C.), and 2-chloro-3-pyridinecarboxylic acid (190 g.). The autoclave was sealed and the reaction mixture heated at 110°C. (50 psig) for 48 hours. The reaction mixture was cooled to 25°C. and discharged from the autoclave. Solids were recovered by filtration. Concentration of the filtrate gave a second crop. These process steps were repeated until virtually all of the methanol had been removed. The several crops of solids were combined, taken up in 2.5 liters of water and acidified with conc. hydrochloric acid to pH 2.7 keeping the temperature below 20°C. The precipitated product was granulated for 30 minutes at 15°C. and recovered by filtration (141 g.). Purified title product was obtained by recrystallization from ethyl acetate-hexane (120.5 g., m.p. 148-150°C.).
7
t V-/ 1
ft ^
P RE P ARATION 3 Ethyl 2-(6-Chloro-8-quinolyl)-2-oxoacetate 8-Bromo-6-chloroquinoline [J. Het. Chem. 6, pp. 243-245 (1969); 6 g., 0.025 mole] in 50 ml. of 5 tetrahydrofuran was added dropwise over a 10 minute period to a mixture of butyl lithium (2.3M in hexane, 12.2 ml., 0.028 mole) and 40 ml. of tetrahydrofuran held at -70°C. After an additional 30 minutes at this temperature, a cold (0°C.) solution of diethyl oxalate 10 (14.6 g., 0.10 mole) in 50 ml. of tetrahydrofuran was added dropwise. The reaction mixture was maintained at 0°C. for 1 hour, then quenched at 0-5°C. with glacial acetic acid (17 ml.) in 50 ml. of tetrahydrofuran.
After warming to room temperature the quenched mixture 15 was poured into 500 ml. of water and then diluted with 5 00 ml. of ethyl acetate and 500 ml. of saturated sodium bicarbonate. The organic layer was separated, washed with 500 ml. of fresh bicarbonate, dried over anhydrous magnesium sulfate, filtered, and evaporated 20 to an oil. Trituration with two 100 ml. portions of hexane gave the title product (2.3 g., m.p. 107-110°C.; m/e 265/263).
# 1978 5 4
PREPARATION 4 Ethyl 2-(6-Chloro-8-quinolyl)-2-hydroxyacetate Sodium borohydride (2.5 g., 0.066 mole) was dissolved in 300 ml. of ethanol at 10°C. and added in one portion to a 10°C. solution of product of the preceding Preparation (2.0 g., 0.0076 mole) in 200 ml. of ethanol. After a few minutes, the reaction mixture was diluted with 750 ml. of ethyl acetate and 750 ml. of water. The aqueous layer was extracted with 250 ml. of fresh ethyl acetate. The organic layers were combined, washed with three 250 ml. portions of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product, initially an oil which crystallized on standing (1.87 g.; m.p. 121-124°C., m/e 267/265).
PREPARATION 5 Ethyl 2-(6-Fluoro-8-quinolyl)-2-oxoacetate By the procedure of Preparation 3, 8-bromo-6-fluoroquinoline [J. Het. Chem., 6, pp. 243-245 (1969); 4.5 g., 0.02 mole] was converted to hexane triturated title product (1.6 g.; m.p. 114-117°C.).
P RE P ARATION 6 Ethyl 2-(6-Fluoro-8-quinolyl)-2-hydroxyacetate By the procedure of Preparation 4, product of the preceding Preparation (1.5 g., 6.1 mmoles) was con-5 verted to title product. The product, initially obtained as a turbid oil, was taken back up in ethyl acetate, washed with brine, dried, filtered and evaporated to an oil which rapidly crystallized (1.23 g., m.p. 84-87°C.). 10 PREPARATION 7
6-Hydroxyquinoline-5-carbaldehyde Sodium hydroxide (25 g.) was dissolved in 35 ml. of water with cooling, 6-hydroxyquinoline (5 g.) in 15 ml. of chloroform was added and the reaction mixture 15 heated to reflux (about 90°C.) for 12 hours, during which two further 15 ml. portions of chloroform were added - one after 2 hours and the other after 6 hours. The reaction mixture was cooled and crude product recovered by filtration. The crude was dissolved in 20 125 ml. of hot water treated with activated carbon,
filtered hot, cooled and acidified with acetic acid and filtered to yield title product [2.5 g.; m.p. 136-137°C.; m/e 173; pnmr/ CDCl^ shows aldehyde proton at 10.5 ppm and aromatic protons at 7.2-9.4 ppm.].
P RE P ARATION 8 6-Methoxyquinoline-5-carbaldehyde Product of the preceding Preparation (1.7 g., 9.8 mmoles) in 8 5 ml. of acetone was combined with potassium carbonate (1.21 g., 8.8 mmoles). Dimethyl sulfate (0.83 ml., 8.8 mmoles) was added and the mixture stirred at room temperature for 16 hours. Additional potassium carbonate (0.34 g., 2.5 mmole) and dimethyl sulfate (0.23 ml., 2.5 mmole) were added and the mixture stirred 4 more hours at room temperature and then 3 hours at 60°C. The reaction mixture was cooled to room temperature, salts removed by filtration, and the filtrate evaporated to dryness. The residue was taken up in ethyl acetate, washed sequentially with two portions of IN ammonium hydroxide, one of water and one of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product [0.78 g.; Rf 0.35 (2:1 ethyl acetate:chloroform); pnmr/CDCl^/delta (ppm): 4.2 (s, 3H), 7.4-9.1 (m, 5H), 10.3 (s, 1H)].
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PREPARATION 9 7-Hydroxyquinoiine-8-carbaldehyde By the procedure of the Preparation 7, 7-hydroxy-quinoline (5 g.) was converted to title product (3.3 g. m.p. 127-130°C.; m/e 173; pnmr/CDCl^ shows aldehyde proton at 10.8 ppm, aromatic protons at 7.0-8.9 ppm.
PREPARATION 10 7-Methoxyquinoline-8-carbaldehyde By the procedure of Preparation 8, the product of the preceding Preparation (3.3 g., 19 mmoles) was converted to title product [2.1 g., pnmr/CDCl^/delta (ppm): 4.1 (s, 3H), 7.5-9.0 (m, 5H), 11.2 (s, 1H)].
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PREPARATION 11 6-Chlorochroman Mossy zinc (75 g.), 7.5 g. of mercuric chloride, 125 ml. of water and 4 ml. of conc. hydrochloric acid 5 were combined, shaken for 5 minutes, allowed to settle, and liquids decanted from the resulting amalgamated zinc. A mixture of 100 ml. of water and 126 ml. of conc. hydrochloric acid and then 6-chloro-4-chomanone (15 g.) were added to the metal, and the mixture re-10 fluxed for 1.5 hours, cooled to room temperature,
decanted from the zinc and the decant extracted with three portions of ether. The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to an oil (14 g.). The oil was chroma-15 tographed on 400 g. of silica gel using 9:1 hexane: ether as eluant tic monitoring and 15 ml. fractions. Clean product fractions were combined and evaporated to yield title product as an oil [8.72 g.; pnmr/CDCl^/ delta (ppm) 2.0 (m, 2H), 3.7 (t, 2H), 4.1 (t, 2H), 6.9 20 (m, 3H); m/e 170/168; Rf 0.88 (2:1 hexane: ether)].
}1 97
P RE P ARATION 12 6-Chlorochroman-8-carbaldehyde Product of the preceding Preparation (8.6 g., 0.051 mole) in 75 ml. of methylene chloride was cooled 5 in an ice-water bath. Titanium tetrachloride (19.34 g.,
11.2 ml., 0.102 mole) was added, followed by the drop-wise addition of 1,1-dichloromethyl methyl ether (6.2 g., 0.054 mole). The reaction mixture was stirred at 0° for 30 minutes, then slowly poured into 400 ml. 10 of saturated sodium bicarbonate. The aqueous phase was extracted with three fresh portions of methylene chloride. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product [7.9 g.; m.p. 83-15 86°C.; pnmr/CDCl3/delta (ppm) 2.0 (m, 2H), 2.8 (t, 2H), 4.2 (t, 2H), 7.1-7.5 (m, 2H), 10.2 (s, 1H), m/e 198/ 196] .
■ 1 97 e 5
PREPARATION 13 6-Fluorochroman By the procedures of Preparation 11, 6-fluoro-4-chromanone (15 g.) was converted to chromatographed 6-5 fluorochroraan [5.7 g.; oil; pnmr/CDCl^/delta (ppm) 2.0 (m, 2H), 3.8 (t, 2H), 4.1 (t, 2H), 6.8 (m, 3H); Rf 0.68 (2:1 hexane:ether); m/e 152],
PREPARATION 14 6-Fluorochroman-8-carbaldehyde 10 By the procedures of Preparation 12, the product of the preceding Preparation (5.5 g., 0.036 mole) was converted to title product initially isolated as a viscous oil which was crystallized from hexane (3.4 g.; m.p. 54-57°C.; m/e 180).
1 97
PREPARATION 15 3-Methyl-5-isoxazolecarboxamide 3-Methyl-5-isoxazolecarboxylic acid (20 g.) was refluxed for 10 hours in 350 ml. of thionyl chloride, 5 then stirred at room temperature for 16 hours, clari fied by filtration and evaporated to an oil. The oil was multiply triturated with hot hexane, and the combined hexane triturates evaporated to yield acid chloride (16.2 to 21 g.) as a solid.
With stirring, acid chloride prepared in the manner (35 g.) was added portionwise to 300 ml. of conc. ammonium hydroxide at room temperature. After granulating for 1 hour, title product was recovered by filtration (24.2 g., m.p. 180-182°C.). 15 PREPARATION 16
3-Methyl-5-isoxazoiecarbonitrile Product of the preceding Preparation (5 g.) was mixed thoroughly with phosphorous pentoxide (10 g.) and placed in an oil bath preheated to 140°. The bath 20 temperature was increased to 200°C. and title product recovered by distillation in vacuo [2.9 g., ir(film) nitrile band at 2220 cm1, no amide peak in the 1700 cm 1 region].
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PREPARATION 17 3-Methyl-5-isoxazoiecarbaldehyde Product of the preceding Preparation (1.08 g., 0.01 mole) was dissolved in 25 ml. of ether and cooled 5 to -40°C. Diisobutylaluminum hydride (12 ml. of 1M in hexane, 0.012 mole) was added at -40°C. over a 15 minute period. The mixture was stirred at -30° to -35°C. for 10 minutes. Keeping the temperature at -20°C., 60 ml. of ethyl acetate was added. Keeping the 10 temperature at -25°C., methanol (15 ml.) was added dropwise, and keeping the temperature below -20°C., 3 ml. of 6N hydrochloric acid was added. The reaction mixture was warmed to 5°C. and the organic phase washed with 25 ml. of water and evaporated to an oil. The oil 15 was chromatographed on 50 ml. of silica gel using 1:1 ether:hexane as eluant. Product fractions were combined and evaporated to yield title product (0.42 g.; m.p. 39-41°C.). A small sample further purified by sublimation had m.p. 43-45°C.
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PREPARATION 18 5-Chlorobenzo[b]furan-2-carboxylic Acid 5-Chlorosalicylaldehyde (31.3 g., 0.2 mole) was dissolved in 200 ml. of 2-butanone. Potassium carbo-5 nate (82.9 g., 0.6 mole) and then diethyl 2-bromo-
malonate (95.6 g., 0.4 mole) were added and the mixture heated to reflux for five hours, then cooled, filtered from salts, and concentrated to an oil. The oil was partitioned between 500 ml. of 10% sulfuric acid and 10 500 ml. of ether. The aqueous layer was extracted with two 250 ml. portions of fresh ether. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to a second oil. The second oil was dissolved in 15 400 ml. of 10% ethanolic potassium hydroxide, heated at reflux for 1 hour and concentrated to solids. The solids were dissolved in 1500 ml. of water, filtered from trace insoluble matter, acidified with 6N hydrochloric acid and precipitated solids recovered by 20 filtration. Purified title product was obtained by repulping the solids in 1 liter of water (19 g., m.p. 259-262°C., m/e 198/196).
By the same procedure, 5-fluorosalicyaldehyde and 6-chlorosalicylaldehyde are converted, respectively, to 25 5-fluorobenzo[b]furan-2-carboxylic acid and 6-chloro-benzo[b]furan-2-carboxylic acid.
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PREPARATION 19 5-Chlorobenzo[b]furan
Title compound of the preceding Preparation (7.8 g.) was combined with copper powder (700 mg.) and guinoline (50 ml.) and the mixture heated to reflux for 50 minutes, then cooled to room temperature and diluted with 500 ml. of ether. Insolubles were removed by filtration and the filtrate washed in sequence with five 200 ml. portions of 2N hydrochloric acid and one of brine, dried over anhydrous magnesium sulfate and concentrated to an oil (6.2 g.). The oil was chromatographed through 200 g. of silica gel using ether as eluant and 300 ml. fractions. Fractions 1 and 2 were combined and evaporated to yield title product as an oil (6.1 g.).
By the same procedure the other benzofurancarboxylic acids of the preceding Preparation are converted to 5-fluorobenzo[b]furan and 6-chlorobenzo[b]furan.
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PREPARATION 20 5-Chloro-2,3-dihydrobenzo[b]furan Pd/C (5%, 12.2 g.) in 400 ml. of acetic acid was prehydrogenated at atmospheric pressure and 25°C.
Title compound of the preceding Preparation (6.1 g.) in 100 ml. of acetic acid was added and hydrogenation continued until slightly more than 1 equivalent of hydrogen had been consumed. Catalyst was recovered by filtration over diatomaceous earth. The filtrate was neutralized with saturated potassium carbonate and extracted with four 200 ml. portions of ether. The combined extracts were washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to an oil. The oil was chromatographed on 400 g. silica gel using hexane-3% ether as eluant, 15 ml. fractions and tic monitoring. Pure product fractions 70-90 were combined and evaporated to yield title product [2.15 g. oil; Rf 0.32 (hexane); m/e 156/154].
By the same procedure, the other benzofurans of the preceding Preparation are converted to 5-fluoro-2,3-dihydrobenzo[b]furan and 6-chloro-2,3-dihydrobenzo [b] furan.
PREPARATION 21 5-Chloro-2,3-dihydroben2Q[b]furan-7-carbaldehyde By the procedure of Preparation 12, title compound of the preceding Preparation (2.1 g.) was converted to 5 crude product contaminated with an isomeric aldehyde. Purified title product was obtained by digesting the crude product in 50 ml. of boiling hexane, filtering and cooling the filtrate [0.93 g.; m.p. 79-81°C.; Rf 0.55 (chloroform); m/e 184/182].
By the same method the 5-fluoro compound of the preceding Preparation is converted to 5-fluoro-2,3-dihydrobenzo[b]furan-7-carbaldehyde.
By the method of Preparation 3, the 6-chloro compound is converted to ethyl 2-(6-chloro-2,3-dihydro-7-15 benzo[b]furanyl)-2-oxoacetate; then by the method of
Preparation 4 to ethyl 2-(6-chloro-2,3-dihydro-7-benzo-[b]furanyl)-2-hydroxyacetate.
1Z73 3 4
-144-PREPARATION 22
7-Chloroquinoline-8-carbaldehyde 7-Chloro-8-methylquinoline (1 g.) [Bradford et al., J. Chem. Soc., p. 437 (1947)] is dissolved in 5 20 ml. of benzene and brominated with one equivalent of N-bromosuccinimide in the presence of catalytic amounts of peroxide. The product, 7-chloro-8-(bromomethyl)-quinoline is isolated by evaporation.
The bromo compound is solvolyzed to 7-chloro-8-10 (hydroxymethyl)quinoline by warming with excess alcoholic potassium hydroxide. To isolate the product, the reaction mixture is neutralized with hydrochloric acid, salts separated by filtration and the filtrate evaporated to dryness.
The alcohol (1 g.) is dissolved in 10 ml. of methylene chloride and added dropwise to a slurry of 1.5 equivalents of pyridinum chlorochromate in 20 ml. of methylene chloride. The exothermic reaction is controlled by rate of addition, use of a reflux con-20 denser and occasional cooling in a cooling bath. The reaction mixture is diluted with ether, and the supernatant separated by decantation and filtration. The product is purified by filtration through a short magnesium silicate column with ether as eluant and 25 isolated by removal of the solvent in vacuo.
PREPARATION 23 3-Furaldehyde 3-Furylmethanol (19.6 g., 0.2 mole) in 50 ml. of methylene chloride was added dropwise to a slurry of 5 pyridinium chlorochromate (64.5 g., 0.3 mole) in
450 ml. of methylene chloride. The exothermic reaction, which led to vigorous reflux, was controlled by occasional cooling with an ice-bath. By the end of 6 0 minutes, gummy solids had precipitated. The 10 reaction mixture was diluted with 600 ml. of ether and the supernatant separated by a combination of decanta-tion and filtration. The filtrate was passed through Florisil (synthetic magnesium silicate) contained in a short column, with ether as eluant. Collected fractions 15 were combined and evaporated to an oil. Distillation of the oil provided 3-furaldehyde (7.6 g.; b.p. 68-72°C./40-45 mm.).
Alternatively, this aldehyde is prepared by Rosenmund reduction of 3-furoic acid chloride [Hayes, 20 J. Am. Chem. Soc. 71, 2581 (1949)].
PREPARATION 24 2-(2-Furyl)-1,3-dioxolane 2-Furaldehyde (42 ml., 0.5 mole), ethyleneglycol (50 ml., 0.9 moles) and p-toluenesulfonic acid (about 25 200 mg.) were combined in 150 ml. of toluene and the mixture refluxed for 6 hours while collecting byproduct water in a Dean-Stark trap. The mixture was cooled, diluted with 500 ml. of ether, and clarified by filtration. The filtrate was washed with 200 ml. 30 of saturated sodium bicarbonate and the organic phase again clarified by filtration. This second filtrate was washed with 200 ml. of water, and the organic layer concentrated to dryness, affording 2-(2-furyl)-1,3-dioxolane as an oil (45 g.).
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PREPARATION 25 2-(5-Chloro-2-furyl)-1,3-dioxolane 2-(2-Furyl)-1,3-dioxolane (14 g., 0.1 mole) was dissolved in 100 ml. of tetrahydrofuran and the 5 solution cooled to -25° to -20°C. Maintaining this temperature range, butyl lithium in hexane (45 ml. of 2.2M, 0.1 mole) was added over a period of 10 minutes. The mixture was allowed to warm to 0°C. over 25 minutes and rechilled to -30°C. While maintaining a 10 temperature range of -30° to -25°C., hexachloroethane (23.7 g., 0.1 mole) in 50 ml. of tetrahydrofuran was added over 5 minutes. The reaction mixture was warmed to room temperature, stirred for 1.5 hours, recooled to 5°C., and diluted slowly with 500 ml. of water. 15 Product was extracted into ether (2 x 500 ml.) and recovered as an oil (15.8 g.) by evaporation to dryness. The oil was chromatographed on a 200 ml. volume of silica gel, using 8:1 hexane:ethyl acetate as eluant and monitoring by silica gel tic with the 20 same eluant. The early, product containing fractions were combined and evaporated to yield purified 2-(5-chloro-2-furyl)-1,3-dioxolane as an oil [5 g.; R^ 0.6 (8:1 hexane:ethyl acetate)].
PREPARATION 26 25 5-Chloro-2-furaldehyde
2-(5-Chloro-2-furyl)-1,3-dioxolane (4.8 g.) was dissolved in 20 ml. of ether. 6N Hydrochloric acid (10 ml.) was added and the two-phase mixture stirred for 1 hour at room temperature. The ether phase was 30 separated, washed with water and evaporated to yield 5-chloro-2-furaldehyde as an oil (2.8 g.).
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PREPARATION 27 5-Bromo-2-furylcarboxamide 5-Bromo-2-furoic acid (20 g.) was refluxed for 3 hours with 60 ml. of thionyl chloride, and the 5 corresponding acid chloride isolated as an oil by concentration. The acid chloride was added dropwise to 150 ml. of stirring, concentrated ammonium hydroxide. Filtration afforded 5-bromo-2-furylcarboxamide (17.0 g., m.p. 140-143°C.). 10 PREPARATION 28
-Bromo-2-furylcarbonitrile 5-Bromo-2-furylcarboxamide (10 g.) was combined with 50 ml. of phosphorus oxychloride and refluxed for 24 hours. The mixture was poured onto ice, the 15 product extracted into ether, which on evaporation gave 5-bromo-2-furylcarbonitrile as an oil (6.4 g.).
PREPARATION 29 5-Bromo-2-furaldehyde 5-Bromo-2-furylcarbonitrile (2.3 g., 13 mmoles) 20 was dissolved in 50 ml. of ether and cooled, under nitrogen, to -10°C. Diisobutylaluminum hydride (1.9 g., 13 mmoles) as a 25% solution in toluene was added dropwise, maintaining the temperature near -10°C. The reaction was allowed to warm to room 25 temperature and allowed to stir about 6 hours. The reaction mixture was cooled to 0° to 5°C., diluted with 1 ml. of methanol, acidified with 3N hydrochloric acid, washed with water, and evaporated to yield 5-bromo-2-furaldehyde (1.2 g., m.p. 74-76°C.).
1978 54
PREP ARATION 30 3-Bromo-2-furaldehyde Phosphorus oxychloride (6.5 g., 7 0 mmoles) was added to dimethylformamide (5.4 g., 70 mmoles) at 0° 5 to 10°C. The resulting slurry was diluted with 10 ml. of ethylene dichloride. Maintaining the mixture near 10°C., 3-bromofuran (9.2 g., 63 mmoles) was added. The reaction mixture was then heated to 58-60°C. for 1 hour and then recooled to 10°C. Sodium acetate 10 trihydrate (15 g.) dissolved in 25 ml. of water was added slowly, with good stirring, keeping the temperature 10° to 30°C. The mixture was reheated to 68-72°C. for 20 minutes, cooled to room temperature, and diluted with 20 ml. of water. Product was extracted 15 into 75 ml. of ether, and the ether back-washed with water and concentrated to yield 3-bromo-2-furaldehyde as an oil [0.9 g., R^ 0.65 (3:1 hexane:ethyl acetate)].
PREPARATION 31 3-Iodofuran
3-Bromofuran (14.7 g., 0.1 mole) in 100 ml. of ether was cooled to -70°C. Butyl lithium (42 ml. of 2.4M, 0.1 mole) in hexane was added dropwise over 0.5 hour, maintaining the temperature from -70° to -65°C. Iodine (25 g., 0.1 mole) in 200 ml. of ether 25 was then added over 1 hour maintaining the same temperature range. The reaction mixture was warmed to room temperature and then back to 2°C. Water (100 ml.) was added dropwise. The ether layer was separated, washed with aqueous thiosulfate and then water, dried 30 over anhydrous sodium sulfate, evaporated to an oil and distilled to yield 3-iodofuran (15.7 g., b.p. 48°/28 mm.).
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PREPARATION 32
3-Methoxyfuran Sodium metal (5.6 g., 0.24 mole) was dissolved in 150 ml. of dry methanol. 3-Iodofuran (15.7 g., 5 0.08 mole) and cuprous oxide (8 g., 0.1 mole) were added and the mixture was refluxed with vigorous stirring for 42 hours. The reaction mixture was cooled to room temperature, diluted with 200 ml. of water, and product extracted into 100 ml. of ether. 10 The ether extract was back-washed with 15 ml. of water, dried over anhydrous sodium sulfate and evaporated to yield crude 3-methoxyfuran (approximately 3-4 g. of approximately 50% purity) suitable for further processing. 15 PREPARATION 33
-Phenyl-2-thenaldehyde 1-Phenylthiophene [1.6 g., 0.01 mole, prepared according to J. Am. Chem. Soc. 46, 2339 (1924)] was dissolved in 20 ml. of tetrahydrofuran and cooled to 20 -40°C. Butyl lithium in hexane (4.5 ml. of 2.2M) was added over 3 minutes, maintaining the temperature -40° to -30°C. The mixture was warmed to 0°C. and then cooled to -40°C. Dimethylformamide (1.2 ml., 15 mmole) was added, maintaining the temperature -40° 25 to-30°C. The mixture was warmed to room temperature and held for 0.5 hour, recooled to 0°C., quenched with 6 ml. of 6N hydrochloric acid, diluted with 10 ml. of water, and extracted with 20 ml. of ether. Evaporation of the ether extract to dryness gave crude 30 product (1.9 g.). Recrystallization from about 35 ml. of hexane gave purified 5-phenyl-2-thenaldehyde (0.9 g., m.p. 90-92°C.).
PREPARATION 34
4-Bromo-3-thenaidehyde 3,4-Dibromothiophene [15 g., 0.062 mole, J. Org. Chem. 36, 2690 (1971)] in 20 ml. of ether was cooled 5 to -70°C. and butyl lithium in hexane (34.8 ml. of
2.1M, 0.073 mole) added dropwise over 5 minutes.
After stirring for 5 minutes at -70°C., the solution was transferred, via nylon tubing under nitrogen pressure, to a solution of dimethylformamide (6.8 g., 10 0.093 mole) in 35 ml. of ether. The resulting mixture was heated to reflux for 2 hours, cooled to room temperature, washed in sequence with two portions of IN hydrochloric acid, one of saturated sodium bicarbonate and one of brine, dried over anhydrous 15 magnesium sulfate, filtered and concentrated to an oil. The oil was twice distilled to yield 4-bromo-3-thenaldehyde (5.7 g., b.p. 81-84°C./0.8 mm., m/e 192/190).
PREPARATION 35 2-Phenylfuran Aniline (46.5 g., 0.5 mole) was combined with 500 ml. of water and 100 ml. of concentrated hydrochloric acid and cooled to -5°C. Sodium nitrite (36.2 g., 0.525 mole) in 100 ml. of water was added dropwise over 45 minutes, keeping the temperature -3° to -5°C. After addition was complete, the mixture was stirred for 30 minutes at -5°C., and zinc chloride (68 g.) was added. Maximal precipitation of the diazonium salt was obtained by the addition of 100 g. of sodium chloride. The mixture was stirred for 5 minutes, with the cooling bath removed and cautiously filtered, without wash, and air dried for 2 hours. (Previous vacuum drying of this product led to explosive decomposition). The intermediate diazonium salt was suspended in 750 ml. of furan at 0°C. With vigorous stirring, powdered sodium hydroxide (5 g.) was added, followed by anhydrous sodium acetate (10 g.). The reaction mixture was stirred for 5 hours at 0°C. and then for 16 hours at room temperature. Solids were removed by filtration and the filtrate evaporated to crude product (25 ml. of oil). Distillation afforded 1-phenylfuran (9.2-9.6 g., b.p. 87-95°/15 mm., b.p. 50°/l mm.).
1
PREPARATION 36 2-Phenyl-2-(2-thienyl)-1,3-dioxolane 2-Benzoylthiophene (19 g., 0.1 mole), ethylene glycol (11 ml., 0.2 mole), toluene (150 ml.) and p-5 toluenesulfonic acid (about 0.2 g.) were combined and refluxed for 6 hours. By-product water was collected in a Dean-Stark trap. Tic (1:8 ethyl acetate:hexane) indicated reaction to be about 40% complete. More ethylene glycol (30 ml.) was added and reflux con-10 tinued for 35 hours. Reaction was still incomplete. The reaction mixture was diluted with 200 ml. of ether, washed twice with 150 ml. portions of water and concentrated to dryness. The residue was chromatographed on about 500 ml. of silica gel, with 1:8 ethyl 15 acetate:hexane as eluant, monitored by tic. Faster moving, product containing fractions were combined and evaporated to yield 2-phenyl-2-(2-thienyl)-l,3-dioxolane [8 g., oil, R^ 0.6 (1:8 ethyl acetate:hexane)].
f978 54
P RE PARATION 37 Methyl 4-Methoxy-3-thenoate Methyl 4-acetoxy-3-thenoate (U.S. Patent 3,144,235; 10 g.) was dissolved in 20 ml. of methanol and added 5 to 100 ml. of methanol containing 0.31 ml. of concentrated sulfuric acid. The mixture was refluxed for 4 days, then neutralized with 0.6 g. of sodium acetate and solvent removed by evaporation. The residue was taken up in 200 ml. of ether. The ether solution was 10 washed sequentially with two 50 ml. portions of water, two 50 ml. portions of IN sodium hydroxide and two 50 ml. portions of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to an oil which crystallized on standing (4.35 g.; m.p. 64-66°C). 15 When this reaction was worked up after only
1 day only a low yield of the desired product (2.2 g) was isolated. The two IN sodium hydroxide extracts were combined and acidified, precipitating methyl 4-hydroxy-3-thenoate (5.13 g.). When this alcohol was 20 dissolved in 100 ml. of methanol containing 0.3 ml. of concentrated sulfuric acid and refluxed for 3 days, the above work-up afforded title product (2.10 g., m.p. 64-66°C.).
i 978 54
PREPARATION 38 1-(4-Methoxy-3-thienyl)methanol Methyl 4-methoxy-3-thenoate (U.S. Patent 4,144,235; 3.9 g., 23 mmoles) was dissolved in 50 ml. of toluene and cooled in an acetone-dry ice bath. Diisobutyl aluminum hydride (46 ml. of 1M in hexane, 46 mmoles) was added dropwise over 30 minutes. The mixture was stirred for an additional 2 hours at the bath temperature and then allowed to warm to room temperature. Keeping the temperature below 30°C., methanol (14.7 g., 18.6 ml., 0.46 mole) was slowly added. The mixture was then stirred for 16 hours at room temperature, by which time a granular precipitate had formed. The mixture was filtered over diatomaceous earth with methanol wash. The combined filtrate and washes were concentrated to yield the title product as an oil (2.8 g., m/e 144).
PREPARATION 39 4-Methoxy-3-thenaldehyde Pyridinium chlorochromate (6.4 g., 29.7 mmoles) was dissolved in 100 ml. of methylene chloride and added in one portion to a solution of the product of the preceding Example (2.8 g., 19.8 mmoles) also in 100 ml. of methylene chloride. The reaction mixture was stirred at room temperature for three hours,
diluted with 200 ml. of ether and decanted from the black precipitate. The precipitate was washed with two 100 ml. portions of ether. The combined decant and washes were filtered, washed in sequence with two portions of IN hydrochloric acid, one portion of water, two portions of IN sodium hydroxide and one portion of brine, dried over anhydrous magnesium sulfate, filtered and concentrated to yield title product as an oil [2.6 g.; m/e 142; ir (CI^Clj)
1688, 1544 cm"1].
197854
PREPARATION 40 Ethyl 4-Ethoxy-3-thenoate Following the approximate procedure of U.S. 4,144,235, methyl 4-acetoxy-3-thenoate (20 g.) was dissolved in 240 ml. of ethanol and 0.62 ml. of concentrated sulfuric acid was added. The reaction mixture was gently refluxed for 79 hours, then neutralized with sodium acetate (1.2 g.) and evaporated to an oil. The latter was partitioned between 400 ml. of ether and 50 ml. of water. The organic layer was separated and washed in sequence with 75 ml. of water, three 50 ml. portions of IN sodium hydroxide' and two 75 ml. portions of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an oil [14.9 g., pnmr indicates entirely ethyl ester, no methyl ester] .
PREPARATION 41 1-(4-Ethoxy-3-thienyl)methanol By the procedure of Preparation 38, the product of the preceding Preparation (14 g.) was converted to title product as an oil (9.15 g.).
PREPARATION 42 4-Ethoxy-3-thenaldehyde By the procedure of Preparation 39, the product of the preceding Preparation (9.15 g.) was converted to the title product, initially isolated as an oil which quickly crystallized on cooling [8.18 g.; m.p. 42-45°C.; m/e 156; ir (KBr) 3090, 2977, 1688 cm"1].
3 975
PREPARATION 43 n-Propyl 4-(n-Propoxy)-3-thenoate By the procedure of Preparation 40, using a reaction reflux time of 10 days, methyl 4-acetoxy-3-thenoate (6 g.) in 750 ml. of 1-propanol containing 0.19 ml. of concentrated sulfuric acid was converted to title product as an oil (5.4 g.; m/e 228).
PREPARATION 44
1-[4-(n-Propoxy)-3-thienyl)methanol 10 By the procedure of Preparation 38, the product of the preceding Preparation (5.4 g.) was reduced to title compound, isolated as an oil (3.44 g.; m/e 172) .
PREPARATION 45 15 4-(n-Propoxy)-3-thenaldehyde)
By the procedure of Preparation 39, the product of the preceding Preparation (3.34 g.) was converted to title compound [3.19 g.; m/e 170; ir (CI^C^) 1689, 1539 cm"1]. 20 PREPARATION 46
Ethyl 4-Methoxy-2-methyl-3-thenoate Ethyl 4-hydroxy-2-methyl-3-thenoate [Chem. Ber. 48, p. 593 (1915); 7.8 g.] was combined with 600 ml. of methanol and 0.25 ml. concentrated sulfuric acid 25 and refluxed for 21 hours. The reaction mixture was evaporated to an oil, taken up in 500 ml. of ether, washed with two 50 ml. portions of IN sodium hydroxide and then one of brine, dried over anhydrous magnesium sulfate, and evaporated to yield title product as an 30 oil (7.8 g.; m/e 200; pnmr/CDCl^ includes singlet
OCH^ protons at 3.9 ppm). The product is contaminated with a minor portion of the corresponding methyl ester.
Claims (9)
1. A racemic or optically active compound of the formula wherein R is hydrogen, (C1-C4)alkanoyl, benzoyl, (C2~C4)-carbalkoxy, (C^-C^)alkylcarbamoyl, (C5~C7)cycloalkyl-carbamoyl or di(C^-C^)alkylcarbamoyl; and (a) or X J VN' R" wherein R' is (C^-C4)alkyl or phenyl, R" is hydrogen, (C^-C4)alkyl or phenyl and X is halo; "tx (b) 1 978 -159- wherein Y is hydrogen or (C^-C^)alkoxy, Y' is hydrogen or (C-^-C-j)alkyl and Y" is hydrogen or halo; (c) Z" or wherein Z' is hydrogen, halo or alkoxy and Z" is hydrogen or halo; <CH2»n t<3) wherein W is hydrogen or halo, and n is 1 or 2; (e) V V—Q IT1 or wherein Q is sulfur or oxygen and V is hydrogen or (C1"C3)alkyl; V (f) fA-!— wherein Q is sulfur or oxygen; and V is hydrogen or (C1-C3)alkyl; or X <g) X1 or r~ 1 97 8 5 -160- wherein Y is sulfur or oxygen; X is hydrogen, halo, methyl, phenyl, benzoyl or (C.. -C,) alkoxy; X1 is hydrogen
2 or methyl; and X is hydrogen or halo; or a pharmaceutically-acceptable cationic salt thereof when R is hydrogen; or a phairmaceutically-acceptable acid addition salt thereof when R1 contains a basic nitrogen functionality. 2. A compound of claim 1 wherein R1 is Y is (C^-C2>alkoxy and Y" is hydrogen, chloro or fluoro.
3. A compound of claim 1 wherein R1 is (CH2)n W is chloro or fluoro, and n is 1 or 2.
4. A compound of claim 1 wherein R1" is and Z" is chloro or fluoro. 5.
A compound of claim 1 wherein R is OCH. rr_ i i X -161- 197854 X is (C,-C2)alkoxy and X is hydrogen or methyl 1
6. A compound of claim 1 wherein R is X II H -o- or and X is hydrogen or halo.
7. A compound of the formula r6—T V OR wherein .2 . R" is (C^-C^)alkyl; and R^ is (a) or wherein R1 is (C^-C4)alkyl or phenyl (b) w (.CH •}) 2 n 1 97854 -162- wherein W is hydrogen or halo, and n is 1 or 2; (c) (Al- wherein Q is sulfur or oxygen; and V is hydrogen or (C1-C3)alkyl; or (d) X or wherein Y is sulfur or oxygen; X is hydrogen# halo, methyl, phenyl, benzoyl or (C^-Cj)alkoxy; X1 is hydrogen or methyl; and is hydrogen or halo. 2 4 MAY 1984 - ]fe& - 19785c
8. A method of lowering the blood glucose level in a hyperglycemic nonhuman mammal which comprises administering a blood glucose level lowering amount of a racemic or optically active compound of claim 1.
9. A method of lowering the blood glucose level in a hyperglycemic nonhuman mammal as claimed in claim 8 substantially as hereinbefore described. DATED TH(8^3^ DAY OF 19®/- A. J. PARK & SON PER AGENTS FOR THE APPLICANTS "X. ' ■ - /•
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17320680A | 1980-07-28 | 1980-07-28 | |
US06/222,202 US4367234A (en) | 1980-07-28 | 1981-01-02 | Hypoglycemic 5-substituted oxazolidine-2,4-diones |
US06/252,962 US4342771A (en) | 1981-01-02 | 1981-04-23 | Hypoglycemic 5-substituted oxazolidine-2,4-diones |
US06/252,961 US4332952A (en) | 1980-07-28 | 1981-04-23 | Hypoglycemic 5-substituted oxazolidine-2,4-diones |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ197854A true NZ197854A (en) | 1984-11-09 |
Family
ID=27497044
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ197854A NZ197854A (en) | 1980-07-28 | 1981-07-27 | 5-substituted oxazolidine-2,4-diones and pharmaceutical compositions |
Country Status (29)
Country | Link |
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JP (1) | JPS5764692A (en) |
AR (3) | AR230053A1 (en) |
AU (2) | AU526733B2 (en) |
CA (1) | CA1161843A (en) |
CH (1) | CH653029A5 (en) |
CS (1) | CS237320B2 (en) |
DD (1) | DD202555A5 (en) |
DE (1) | DE3129275A1 (en) |
DK (1) | DK152650C (en) |
ES (4) | ES504321A0 (en) |
FI (1) | FI75820C (en) |
FR (1) | FR2487350B1 (en) |
GB (5) | GB2080803B (en) |
GR (1) | GR75303B (en) |
HK (1) | HK43886A (en) |
IE (1) | IE51662B1 (en) |
IL (1) | IL63424A (en) |
IT (1) | IT1138111B (en) |
KE (1) | KE3624A (en) |
LU (1) | LU83513A1 (en) |
MY (1) | MY8600596A (en) |
NO (1) | NO812559L (en) |
NZ (1) | NZ197854A (en) |
PH (2) | PH21172A (en) |
PL (1) | PL133220B1 (en) |
PT (1) | PT73436B (en) |
SE (1) | SE461039B (en) |
SG (1) | SG56656G (en) |
YU (2) | YU185481A (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4689336A (en) * | 1981-01-02 | 1987-08-25 | Pfizer Inc. | Hypoglycemic 5-substituted oxazolidine 2,4-diones |
US4695634A (en) * | 1981-01-02 | 1987-09-22 | Pfizer Inc. | Hypoglycemic 5-substituted oxazolidine-2,4-diones |
GR78120B (en) * | 1982-03-01 | 1984-09-26 | Pfizer | |
DE3233089A1 (en) * | 1982-09-07 | 1984-03-08 | Basf Ag, 6700 Ludwigshafen | CHINOLINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH |
JPS59152382A (en) * | 1983-02-18 | 1984-08-31 | Tanabe Seiyaku Co Ltd | Furyloxazolylacetic acid derivative and its preparation |
US4968707A (en) * | 1987-06-10 | 1990-11-06 | Pfizer Inc. | Oxazolidin-2-one derivatives as hypoglycemic agents |
TW403748B (en) | 1994-11-02 | 2000-09-01 | Takeda Chemical Industries Ltd | An oxazolidinedione derivative, its production and a pharmaceutical composition for lowering blood sugar and lipid in blood comprising the same |
IL117208A0 (en) * | 1995-02-23 | 1996-06-18 | Nissan Chemical Ind Ltd | Indole type thiazolidines |
HUE027546T2 (en) | 2003-08-29 | 2016-10-28 | Brigham & Womens Hospital Inc | Hydantoin derivatives as inhibitors of cellular necrosis |
WO2008154484A1 (en) * | 2007-06-08 | 2008-12-18 | Mannkind Corporation | Ire-1a inhibitors |
CA2772760A1 (en) | 2008-12-23 | 2010-07-01 | President And Fellows Of Harvard College | Small molecule inhibitors of necroptosis |
WO2014145022A1 (en) | 2013-03-15 | 2014-09-18 | President And Fellows Of Harvard College | Hybrid necroptosis inhibitors |
AU2015360291A1 (en) | 2014-12-11 | 2017-07-13 | President And Fellows Of Harvard College | Inhibitors of cellular necrosis and related methods |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE729852C (en) * | 1939-07-06 | 1943-01-04 | Carl Nachtigall | Process for the preparation of 2,4-dioxooxazolidines |
DE834992C (en) * | 1946-09-16 | 1952-03-27 | British Schering Res Lab Ltd | Process for the preparation of N-alkyl or N-aralkyl derivatives of oxazolidine-2, 4-dynes |
US2721197A (en) * | 1953-01-05 | 1955-10-18 | Bristol Lab Inc | Bicyclic lactams |
US2954381A (en) * | 1958-12-03 | 1960-09-27 | Us Vitamin Pharm Corp | Heteroaryloxazolidinediones |
US3699229A (en) * | 1970-12-18 | 1972-10-17 | Abbott Lab | 2-oxo-5-phenyl-4-oxazolidinone as an anti-depressant agent |
DE2813873A1 (en) * | 1978-03-31 | 1979-10-11 | Basf Ag | PROCESS FOR THE PRODUCTION OF OXAZOLIDINE-2,4-DIONEN |
US4200642A (en) * | 1978-08-21 | 1980-04-29 | Pfizer Inc. | Spiro-oxazolidindiones |
-
1981
- 1981-07-22 GB GB8122524A patent/GB2080803B/en not_active Expired
- 1981-07-22 SG SG305/86A patent/SG56656G/en unknown
- 1981-07-23 PL PL1981232330A patent/PL133220B1/en unknown
- 1981-07-23 CS CS815646A patent/CS237320B2/en unknown
- 1981-07-24 DE DE19813129275 patent/DE3129275A1/en active Granted
- 1981-07-24 SE SE8104543A patent/SE461039B/en not_active IP Right Cessation
- 1981-07-27 DK DK334781A patent/DK152650C/en not_active IP Right Cessation
- 1981-07-27 FR FR8114542A patent/FR2487350B1/en not_active Expired
- 1981-07-27 GR GR65638A patent/GR75303B/el unknown
- 1981-07-27 NZ NZ197854A patent/NZ197854A/en unknown
- 1981-07-27 ES ES504321A patent/ES504321A0/en active Granted
- 1981-07-27 IL IL63424A patent/IL63424A/en unknown
- 1981-07-27 IE IE1696/81A patent/IE51662B1/en unknown
- 1981-07-27 PT PT73436A patent/PT73436B/en unknown
- 1981-07-27 IT IT23176/81A patent/IT1138111B/en active
- 1981-07-27 AU AU73436/81A patent/AU526733B2/en not_active Ceased
- 1981-07-27 NO NO812559A patent/NO812559L/en unknown
- 1981-07-27 PH PH25966A patent/PH21172A/en unknown
- 1981-07-27 YU YU01854/81A patent/YU185481A/en unknown
- 1981-07-27 LU LU83513A patent/LU83513A1/en unknown
- 1981-07-27 JP JP56117572A patent/JPS5764692A/en active Granted
- 1981-07-27 CH CH4878/81A patent/CH653029A5/en not_active IP Right Cessation
- 1981-07-27 DD DD81232129A patent/DD202555A5/en unknown
- 1981-07-27 FI FI812339A patent/FI75820C/en not_active IP Right Cessation
- 1981-07-27 CA CA000382568A patent/CA1161843A/en not_active Expired
-
1982
- 1982-04-27 AR AR289218A patent/AR230053A1/en active
- 1982-04-27 AR AR289216A patent/AR230281A1/en active
- 1982-04-27 AR AR289217A patent/AR229958A1/en active
- 1982-07-23 ES ES514314A patent/ES8306147A1/en not_active Expired
- 1982-07-23 ES ES514315A patent/ES8306148A1/en not_active Expired
- 1982-07-23 ES ES514316A patent/ES8305760A1/en not_active Expired
- 1982-11-02 AU AU90100/82A patent/AU548932B2/en not_active Ceased
-
1983
- 1983-01-03 PH PH28343A patent/PH18925A/en unknown
- 1983-04-22 YU YU00919/83A patent/YU91983A/en unknown
- 1983-06-24 GB GB08317146A patent/GB2131422B/en not_active Expired
- 1983-06-24 GB GB08317147A patent/GB2128184B/en not_active Expired
- 1983-06-24 GB GB08317142A patent/GB2134104B/en not_active Expired
- 1983-06-24 GB GB08317143A patent/GB2134105B/en not_active Expired
-
1986
- 1986-04-04 KE KE3624A patent/KE3624A/en unknown
- 1986-06-09 HK HK438/86A patent/HK43886A/en unknown
- 1986-12-30 MY MY596/86A patent/MY8600596A/en unknown
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