JPH0262547B2 - - Google Patents
Info
- Publication number
- JPH0262547B2 JPH0262547B2 JP1302281A JP30228189A JPH0262547B2 JP H0262547 B2 JPH0262547 B2 JP H0262547B2 JP 1302281 A JP1302281 A JP 1302281A JP 30228189 A JP30228189 A JP 30228189A JP H0262547 B2 JPH0262547 B2 JP H0262547B2
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- evaporated
- ethyl acetate
- trifluoroethyl
- dryness
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000004434 sulfur atom Chemical group 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical group C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 claims 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 209
- 239000000203 mixture Substances 0.000 description 102
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 100
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 96
- 235000019439 ethyl acetate Nutrition 0.000 description 71
- 239000000243 solution Substances 0.000 description 67
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 58
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 48
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 38
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 36
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- 150000001875 compounds Chemical class 0.000 description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
- 239000000706 filtrate Substances 0.000 description 23
- -1 3,4-dioxocyclobutene-1,2-diyl group Chemical group 0.000 description 22
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 21
- 238000010992 reflux Methods 0.000 description 20
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 19
- 235000019341 magnesium sulphate Nutrition 0.000 description 19
- 239000007787 solid Substances 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 239000000725 suspension Substances 0.000 description 15
- SUNMBRGCANLOEG-UHFFFAOYSA-N 1,3-dichloroacetone Chemical compound ClCC(=O)CCl SUNMBRGCANLOEG-UHFFFAOYSA-N 0.000 description 14
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 14
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 14
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 13
- 238000003756 stirring Methods 0.000 description 13
- 229920006395 saturated elastomer Polymers 0.000 description 12
- GOXVPASJCHROBY-UHFFFAOYSA-N 1,1,1-trifluoro-2-isothiocyanatoethane Chemical compound FC(F)(F)CN=C=S GOXVPASJCHROBY-UHFFFAOYSA-N 0.000 description 11
- 239000010410 layer Substances 0.000 description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 229910021529 ammonia Inorganic materials 0.000 description 10
- 239000008346 aqueous phase Substances 0.000 description 10
- 239000000284 extract Substances 0.000 description 10
- 238000002844 melting Methods 0.000 description 10
- 230000008018 melting Effects 0.000 description 10
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 8
- IXBPPZBJIFNGJJ-UHFFFAOYSA-N sodium;cyanoiminomethylideneazanide Chemical compound [Na+].N#C[N-]C#N IXBPPZBJIFNGJJ-UHFFFAOYSA-N 0.000 description 8
- YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 description 8
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 8
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
- OGMADIBCHLQMIP-UHFFFAOYSA-N 2-aminoethanethiol;hydron;chloride Chemical compound Cl.NCCS OGMADIBCHLQMIP-UHFFFAOYSA-N 0.000 description 7
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 7
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 7
- 239000002024 ethyl acetate extract Substances 0.000 description 7
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
- 229910000474 mercury oxide Inorganic materials 0.000 description 7
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 239000011976 maleic acid Substances 0.000 description 6
- 239000012044 organic layer Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 125000006239 protecting group Chemical group 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- QGVJGVSOYVPOGX-UHFFFAOYSA-N [n'-(2,2,2-trifluoroethyl)carbamimidoyl]thiourea Chemical compound NC(=S)NC(=N)NCC(F)(F)F QGVJGVSOYVPOGX-UHFFFAOYSA-N 0.000 description 5
- 239000012259 ether extract Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 102000005962 receptors Human genes 0.000 description 5
- 108020003175 receptors Proteins 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 4
- 150000002357 guanidines Chemical class 0.000 description 4
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000003039 volatile agent Substances 0.000 description 4
- KWPQTFXULUUCGD-UHFFFAOYSA-N 3,4,5,7,8,9,10,10a-octahydropyrido[1,2-a][1,4]diazepine Chemical compound C1CCN=CC2CCCCN21 KWPQTFXULUUCGD-UHFFFAOYSA-N 0.000 description 3
- DCPSTSVLRXOYGS-UHFFFAOYSA-N 6-amino-1h-pyrimidine-2-thione Chemical compound NC1=CC=NC(S)=N1 DCPSTSVLRXOYGS-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 239000006286 aqueous extract Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Chemical group 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 3
- 229960001340 histamine Drugs 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000006188 syrup Substances 0.000 description 3
- 235000020357 syrup Nutrition 0.000 description 3
- PXZDQCNDYUWQGI-UHFFFAOYSA-N (2-chloro-2,2-difluoroethyl)azanium;chloride Chemical compound Cl.NCC(F)(F)Cl PXZDQCNDYUWQGI-UHFFFAOYSA-N 0.000 description 2
- YGMPMXTWKROXPP-UHFFFAOYSA-N (6-aminopyridin-2-yl)methanol Chemical compound NC1=CC=CC(CO)=N1 YGMPMXTWKROXPP-UHFFFAOYSA-N 0.000 description 2
- KWXFSKMBUCYCQW-UHFFFAOYSA-N 1-(2-methylsulfanylpyrimidin-4-yl)-2-(2,2,2-trifluoroethyl)guanidine Chemical compound CSC1=NC=CC(NC(N)=NCC(F)(F)F)=N1 KWXFSKMBUCYCQW-UHFFFAOYSA-N 0.000 description 2
- QZULBUIYVBOYON-UHFFFAOYSA-N 1-(2-methylsulfinylpyrimidin-4-yl)-2-(2,2,2-trifluoroethyl)guanidine Chemical compound CS(=O)C1=NC=CC(NC(N)=NCC(F)(F)F)=N1 QZULBUIYVBOYON-UHFFFAOYSA-N 0.000 description 2
- SCVHSDJRYRGIOY-UHFFFAOYSA-N 1-[1-(2-cyanoethyl)pyrazol-3-yl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound FC(F)(F)CNC(=S)NC=1C=CN(CCC#N)N=1 SCVHSDJRYRGIOY-UHFFFAOYSA-N 0.000 description 2
- HDYYRIYUIJDEEE-UHFFFAOYSA-N 1-[2-[2-(1,3-dioxoisoindol-2-yl)ethylsulfanyl]pyrimidin-4-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC1=CC=NC(SCCN2C(C3=CC=CC=C3C2=O)=O)=N1 HDYYRIYUIJDEEE-UHFFFAOYSA-N 0.000 description 2
- GNXXPUACTLKRRK-UHFFFAOYSA-N 1-[2-[2-(1,3-dioxoisoindol-2-yl)ethylsulfanylmethyl]pyrimidin-4-yl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound FC(F)(F)CNC(=S)NC1=CC=NC(CSCCN2C(C3=CC=CC=C3C2=O)=O)=N1 GNXXPUACTLKRRK-UHFFFAOYSA-N 0.000 description 2
- NWKIODFPRAEIBS-UHFFFAOYSA-N 1-[4-(2-aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSCC1=CSC(NC(N)=NCC(F)(F)F)=N1 NWKIODFPRAEIBS-UHFFFAOYSA-N 0.000 description 2
- KGPSVPZEXNFNLG-UHFFFAOYSA-N 1-[4-[4-(1,3-dioxoisoindol-2-yl)butyl]-1,3-thiazol-2-yl]-2-(2,2,2-trifluoroethyl)guanidine;hydrochloride Chemical compound Cl.S1C(NC(N)=NCC(F)(F)F)=NC(CCCCN2C(C3=CC=CC=C3C2=O)=O)=C1 KGPSVPZEXNFNLG-UHFFFAOYSA-N 0.000 description 2
- XBGBDXZDRASPFK-UHFFFAOYSA-N 1-[6-(hydroxymethyl)pyridin-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC1=CC=CC(CO)=N1 XBGBDXZDRASPFK-UHFFFAOYSA-N 0.000 description 2
- 125000000453 2,2,2-trichloroethyl group Chemical group [H]C([H])(*)C(Cl)(Cl)Cl 0.000 description 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- 125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 description 2
- RPFBEKFUFFMCHS-UHFFFAOYSA-N 2-(6-chloro-5-oxohexyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCC(=O)CCl)C(=O)C2=C1 RPFBEKFUFFMCHS-UHFFFAOYSA-N 0.000 description 2
- JWAQENUKTAOJST-UHFFFAOYSA-N 2-(chloromethyl)pyrimidin-4-amine Chemical compound NC1=CC=NC(CCl)=N1 JWAQENUKTAOJST-UHFFFAOYSA-N 0.000 description 2
- XWHFPQYLXVMCGP-UHFFFAOYSA-N 2-[2-(4-aminopyrimidin-2-yl)sulfanylethyl]isoindole-1,3-dione Chemical compound NC1=CC=NC(SCCN2C(C3=CC=CC=C3C2=O)=O)=N1 XWHFPQYLXVMCGP-UHFFFAOYSA-N 0.000 description 2
- VHWPOODFQBOEQR-UHFFFAOYSA-N 2-[2-[(4-aminopyrimidin-2-yl)methylsulfanyl]ethyl]isoindole-1,3-dione Chemical compound NC1=CC=NC(CSCCN2C(C3=CC=CC=C3C2=O)=O)=N1 VHWPOODFQBOEQR-UHFFFAOYSA-N 0.000 description 2
- BQMOOFFLOYIQKM-UHFFFAOYSA-N 2-[4-(4-aminopyrimidin-2-yl)sulfanylbutyl]isoindole-1,3-dione Chemical compound NC1=CC=NC(SCCCCN2C(C3=CC=CC=C3C2=O)=O)=N1 BQMOOFFLOYIQKM-UHFFFAOYSA-N 0.000 description 2
- 125000004780 2-chloro-2,2-difluoroethyl group Chemical group [H]C([H])(*)C(F)(F)Cl 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- OKGXJRGLYVRVNE-UHFFFAOYSA-N diaminomethylidenethiourea Chemical compound NC(N)=NC(N)=S OKGXJRGLYVRVNE-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 229940101209 mercuric oxide Drugs 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- OJZQOQNSUZLSMV-UHFFFAOYSA-N (3-aminophenyl)methanol Chemical compound NC1=CC=CC(CO)=C1 OJZQOQNSUZLSMV-UHFFFAOYSA-N 0.000 description 1
- SNMLKBMPULDPTA-UHFFFAOYSA-N 1,1,1-trifluoropropan-2-amine Chemical compound CC(N)C(F)(F)F SNMLKBMPULDPTA-UHFFFAOYSA-N 0.000 description 1
- BGNORAQHPDCDDJ-UHFFFAOYSA-N 1,2,3,4,6,7,8,10a-octahydropyrimido[1,2-a]azepine Chemical compound C1=CCCCN2CCCNC21 BGNORAQHPDCDDJ-UHFFFAOYSA-N 0.000 description 1
- YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical group C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 description 1
- QUDQPJZMLWYGJH-UHFFFAOYSA-N 1-(2-methylsulfanylpyrimidin-4-yl)-3-(2,2,2-trifluoroethyl)thiourea Chemical compound CSC1=NC=CC(NC(=S)NCC(F)(F)F)=N1 QUDQPJZMLWYGJH-UHFFFAOYSA-N 0.000 description 1
- KIRKIQMOQXADDF-UHFFFAOYSA-N 1-(6-chloropyrazin-2-yl)-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC1=CN=CC(Cl)=N1 KIRKIQMOQXADDF-UHFFFAOYSA-N 0.000 description 1
- HKUMEEMCVVPKGN-UHFFFAOYSA-N 1-[1-(2-cyanoethyl)pyrazol-3-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC=1C=CN(CCC#N)N=1 HKUMEEMCVVPKGN-UHFFFAOYSA-N 0.000 description 1
- VEVSWYOIMUSNLU-UHFFFAOYSA-N 1-[1-(3-aminopropyl)pyrazol-3-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCCN1C=CC(NC(N)=NCC(F)(F)F)=N1 VEVSWYOIMUSNLU-UHFFFAOYSA-N 0.000 description 1
- AYRZOLQGFHQWLW-UHFFFAOYSA-N 1-[2-(2-aminoethylsulfanyl)pyrimidin-4-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSC1=NC=CC(NC(N)=NCC(F)(F)F)=N1 AYRZOLQGFHQWLW-UHFFFAOYSA-N 0.000 description 1
- WVRCYXCWGORVCA-UHFFFAOYSA-N 1-[2-(2-aminoethylsulfanylmethyl)pyrimidin-4-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSCC1=NC=CC(NC(N)=NCC(F)(F)F)=N1 WVRCYXCWGORVCA-UHFFFAOYSA-N 0.000 description 1
- NVLCGFFLOKLKDF-UHFFFAOYSA-N 1-[2-(3-aminopropylamino)pyrimidin-4-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCCNC1=NC=CC(NC(N)=NCC(F)(F)F)=N1 NVLCGFFLOKLKDF-UHFFFAOYSA-N 0.000 description 1
- SBLXFIBRVBFITQ-UHFFFAOYSA-N 1-[2-(4-aminobutylsulfanyl)pyrimidin-4-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCCCSC1=NC=CC(NC(N)=NCC(F)(F)F)=N1 SBLXFIBRVBFITQ-UHFFFAOYSA-N 0.000 description 1
- HTGGJDWNEGELCK-UHFFFAOYSA-N 1-[2-[2-(1,3-dioxoisoindol-2-yl)ethylsulfanyl]pyrimidin-4-yl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound FC(F)(F)CNC(=S)NC1=CC=NC(SCCN2C(C3=CC=CC=C3C2=O)=O)=N1 HTGGJDWNEGELCK-UHFFFAOYSA-N 0.000 description 1
- ONSYNRRLIJVJMT-UHFFFAOYSA-N 1-[2-[3-(1,3-dioxoisoindol-2-yl)propylsulfanyl]pyrimidin-4-yl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound FC(F)(F)CNC(=S)NC1=CC=NC(SCCCN2C(C3=CC=CC=C3C2=O)=O)=N1 ONSYNRRLIJVJMT-UHFFFAOYSA-N 0.000 description 1
- QZDUZEASXAYKHF-UHFFFAOYSA-N 1-[2-[4-(1,3-dioxoisoindol-2-yl)butylsulfanyl]pyrimidin-4-yl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound FC(F)(F)CNC(=S)NC1=CC=NC(SCCCCN2C(C3=CC=CC=C3C2=O)=O)=N1 QZDUZEASXAYKHF-UHFFFAOYSA-N 0.000 description 1
- JQEXWJNXXXXODH-UHFFFAOYSA-N 1-[3-(2-aminoethylsulfanylmethyl)-1,2,4-thiadiazol-5-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSCC1=NSC(NC(N)=NCC(F)(F)F)=N1 JQEXWJNXXXXODH-UHFFFAOYSA-N 0.000 description 1
- RAVIOCFHAWLFJD-UHFFFAOYSA-N 1-[3-(2-aminoethylsulfanylmethyl)phenyl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSCC1=CC=CC(NC(=N)NCC(F)(F)F)=C1 RAVIOCFHAWLFJD-UHFFFAOYSA-N 0.000 description 1
- RBZSNOBDEMUSRS-UHFFFAOYSA-N 1-[3-(chloromethyl)-1,2,4-thiadiazol-5-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC1=NC(CCl)=NS1 RBZSNOBDEMUSRS-UHFFFAOYSA-N 0.000 description 1
- FHDQQJRQWWEZJB-UHFFFAOYSA-N 1-[3-(chloromethyl)phenyl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CNC(=N)NC1=CC=CC(CCl)=C1 FHDQQJRQWWEZJB-UHFFFAOYSA-N 0.000 description 1
- HYMFZSBUWKKBRW-UHFFFAOYSA-N 1-[3-(hydroxymethyl)-1,2,4-thiadiazol-5-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound FC(F)(F)CN=C(N)NC1=NC(CO)=NS1 HYMFZSBUWKKBRW-UHFFFAOYSA-N 0.000 description 1
- RASDFQMHBZCXKT-UHFFFAOYSA-N 1-[3-(hydroxymethyl)phenyl]-3-(2,2,2-trifluoroethyl)thiourea Chemical compound OCC1=CC=CC(NC(=S)NCC(F)(F)F)=C1 RASDFQMHBZCXKT-UHFFFAOYSA-N 0.000 description 1
- JAWSVXXFNSCEQD-UHFFFAOYSA-N 1-[4-(2-aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]-2-(2,2,2-trichloroethyl)guanidine Chemical compound NCCSCC1=CSC(NC(N)=NCC(Cl)(Cl)Cl)=N1 JAWSVXXFNSCEQD-UHFFFAOYSA-N 0.000 description 1
- PSSKAMLFOAWLQX-UHFFFAOYSA-N 1-[4-(2-aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]-2-(2,2,3,3,3-pentafluoropropyl)guanidine Chemical compound NCCSCC1=CSC(NC(N)=NCC(F)(F)C(F)(F)F)=N1 PSSKAMLFOAWLQX-UHFFFAOYSA-N 0.000 description 1
- PRQXEAOYRQKQLI-UHFFFAOYSA-N 1-[4-(2-aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]-2-(2,2,3,3-tetrafluoropropyl)guanidine Chemical compound NCCSCC1=CSC(NC(N)=NCC(F)(F)C(F)F)=N1 PRQXEAOYRQKQLI-UHFFFAOYSA-N 0.000 description 1
- RWOBHIDGGMYGDW-UHFFFAOYSA-N 1-[4-(2-aminoethylsulfanylmethyl)-1,3-thiazol-2-yl]-2-(2,2-difluoroethyl)guanidine Chemical compound NCCSCC1=CSC(NC(N)=NCC(F)F)=N1 RWOBHIDGGMYGDW-UHFFFAOYSA-N 0.000 description 1
- MDNHLFUZGIMIIC-UHFFFAOYSA-N 1-[4-(4-aminobutyl)-1,3-thiazol-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCCCC1=CSC(NC(N)=NCC(F)(F)F)=N1 MDNHLFUZGIMIIC-UHFFFAOYSA-N 0.000 description 1
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- VMMBBFNVXODZMF-UHFFFAOYSA-N 1-[6-(2-aminoethylsulfanyl)pyrazin-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSC1=CN=CC(NC(N)=NCC(F)(F)F)=N1 VMMBBFNVXODZMF-UHFFFAOYSA-N 0.000 description 1
- ORCCLKCYCUHNRT-UHFFFAOYSA-N 1-[6-(2-aminoethylsulfanylmethyl)pyridin-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCSCC1=CC=CC(NC(N)=NCC(F)(F)F)=N1 ORCCLKCYCUHNRT-UHFFFAOYSA-N 0.000 description 1
- VDZKMHRFRQDAKX-UHFFFAOYSA-N 1-[6-(3-aminopropylsulfanyl)pyrazin-2-yl]-2-(2,2,2-trifluoroethyl)guanidine Chemical compound NCCCSC1=CN=CC(NC(N)=NCC(F)(F)F)=N1 VDZKMHRFRQDAKX-UHFFFAOYSA-N 0.000 description 1
- IQYOCAULRRSZTK-UHFFFAOYSA-N 2,2,2-trichloroethanamine;hydrochloride Chemical compound Cl.NCC(Cl)(Cl)Cl IQYOCAULRRSZTK-UHFFFAOYSA-N 0.000 description 1
- XALAKNVRDOVOGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-amine;hydrochloride Chemical compound Cl.NCC(F)(F)C(F)F XALAKNVRDOVOGD-UHFFFAOYSA-N 0.000 description 1
- 125000004781 2,2-dichloro-2-fluoroethyl group Chemical group [H]C([H])(*)C(F)(Cl)Cl 0.000 description 1
- YSVKPVHTHFECBE-UHFFFAOYSA-N 2,2-difluoroethanamine;hydrochloride Chemical compound Cl.NCC(F)F YSVKPVHTHFECBE-UHFFFAOYSA-N 0.000 description 1
- CHZXTOCAICMPQR-UHFFFAOYSA-N 2-(2-bromoethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCBr)C(=O)C2=C1 CHZXTOCAICMPQR-UHFFFAOYSA-N 0.000 description 1
- UHOPWFKONJYLCF-UHFFFAOYSA-N 2-(2-sulfanylethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCS)C(=O)C2=C1 UHOPWFKONJYLCF-UHFFFAOYSA-N 0.000 description 1
- VKJCJJYNVIYVQR-UHFFFAOYSA-N 2-(3-bromopropyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCBr)C(=O)C2=C1 VKJCJJYNVIYVQR-UHFFFAOYSA-N 0.000 description 1
- UXFWTIGUWHJKDD-UHFFFAOYSA-N 2-(4-bromobutyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCBr)C(=O)C2=C1 UXFWTIGUWHJKDD-UHFFFAOYSA-N 0.000 description 1
- ZDMJVZQTAJYNPF-UHFFFAOYSA-N 2-(6-chloro-5-oxoheptyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCC(=O)C(Cl)C)C(=O)C2=C1 ZDMJVZQTAJYNPF-UHFFFAOYSA-N 0.000 description 1
- GYCIODFTXTYNRO-UHFFFAOYSA-N 2-(7-chloro-6-oxoheptyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCCCCC(=O)CCl)C(=O)C2=C1 GYCIODFTXTYNRO-UHFFFAOYSA-N 0.000 description 1
- DMNGMPOYVJPVSK-UHFFFAOYSA-N 2-(oxan-2-yloxy)ethanimidamide;hydrochloride Chemical compound Cl.NC(=N)COC1CCCCO1 DMNGMPOYVJPVSK-UHFFFAOYSA-N 0.000 description 1
- HUHXLHLWASNVDB-UHFFFAOYSA-N 2-(oxan-2-yloxy)oxane Chemical group O1CCCCC1OC1OCCCC1 HUHXLHLWASNVDB-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- PSAKKOKLSDIKEK-UHFFFAOYSA-N 2-chloro-2,2-difluoroacetamide Chemical compound NC(=O)C(F)(F)Cl PSAKKOKLSDIKEK-UHFFFAOYSA-N 0.000 description 1
- 125000004779 2-chloro-2-fluoroethyl group Chemical group [H]C([H])(*)C([H])(F)Cl 0.000 description 1
- GUPOZVHRTJYZCX-UHFFFAOYSA-N 2-chloroethanimidamide;hydron;chloride Chemical compound [Cl-].NC(=[NH2+])CCl GUPOZVHRTJYZCX-UHFFFAOYSA-N 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
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- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- QXJJFPIFCZGXGR-UHFFFAOYSA-N 2-methyl-1,3-thiazol-3-ium;chloride Chemical compound Cl.CC1=NC=CS1 QXJJFPIFCZGXGR-UHFFFAOYSA-N 0.000 description 1
- HGGXLEAHOVIYKT-UHFFFAOYSA-N 2-methylsulfanylpyrimidin-4-amine Chemical compound CSC1=NC=CC(N)=N1 HGGXLEAHOVIYKT-UHFFFAOYSA-N 0.000 description 1
- MHMTZDHAMDKMIJ-UHFFFAOYSA-N 3-(3-aminopyrazol-1-yl)propanenitrile Chemical compound NC=1C=CN(CCC#N)N=1 MHMTZDHAMDKMIJ-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- YZUQMEFYKXKFBZ-UHFFFAOYSA-N 3-n-(2,2,2-trifluoroethyl)-1,2,4-thiadiazole-3,5-diamine Chemical compound NC1=NC(NCC(F)(F)F)=NS1 YZUQMEFYKXKFBZ-UHFFFAOYSA-N 0.000 description 1
- TUPWSWLJDSELPV-UHFFFAOYSA-N 3-n-(2,2,2-trifluoroethyl)-1,2,4-thiadiazole-3,5-diamine;hydrobromide Chemical compound Br.NC1=NC(NCC(F)(F)F)=NS1 TUPWSWLJDSELPV-UHFFFAOYSA-N 0.000 description 1
- GMEDUXHKSSWXSL-UHFFFAOYSA-N 3-sulfanylpropylazanium;chloride Chemical compound Cl.NCCCS GMEDUXHKSSWXSL-UHFFFAOYSA-N 0.000 description 1
- SXXLKZCNJHJYFL-UHFFFAOYSA-N 4,5,6,7-tetrahydro-[1,2]oxazolo[4,5-c]pyridin-5-ium-3-olate Chemical compound C1CNCC2=C1ONC2=O SXXLKZCNJHJYFL-UHFFFAOYSA-N 0.000 description 1
- NMCKJFCJIHCHIS-UHFFFAOYSA-N 6-aminopyridine-2-carboxylic acid Chemical compound NC1=CC=CC(C(O)=O)=N1 NMCKJFCJIHCHIS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000004694 Eucalyptus leucoxylon Nutrition 0.000 description 1
- 244000166102 Eucalyptus leucoxylon Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 102000000543 Histamine Receptors Human genes 0.000 description 1
- 108010002059 Histamine Receptors Proteins 0.000 description 1
- 101000799461 Homo sapiens Thrombopoietin Proteins 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 102100034195 Thrombopoietin Human genes 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000000460 chlorine Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- CCGSUNCLSOWKJO-UHFFFAOYSA-N cimetidine Chemical compound N#CNC(=N/C)\NCCSCC1=NC=N[C]1C CCGSUNCLSOWKJO-UHFFFAOYSA-N 0.000 description 1
- 229960001380 cimetidine Drugs 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 230000027119 gastric acid secretion Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003485 histamine H2 receptor antagonist Substances 0.000 description 1
- ZTUJDPKOHPKRMO-UHFFFAOYSA-N hydron;2,2,2-trifluoroethanamine;chloride Chemical compound Cl.NCC(F)(F)F ZTUJDPKOHPKRMO-UHFFFAOYSA-N 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- YECBIJXISLIIDS-UHFFFAOYSA-N mepyramine Chemical compound C1=CC(OC)=CC=C1CN(CCN(C)C)C1=CC=CC=N1 YECBIJXISLIIDS-UHFFFAOYSA-N 0.000 description 1
- 229960000582 mepyramine Drugs 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- 125000005543 phthalimide group Chemical class 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/43—Y being a hetero atom
- C07C323/44—X or Y being nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/24—Derivatives of thiourea containing any of the groups, X being a hetero atom, Y being any atom
- C07C335/28—Y being a hetero atom, e.g. thiobiuret
-
- 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings 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
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings 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
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/48—Acylated amino or imino radicals by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof, e.g. carbonylguanidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/08—1,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7939232 | 1979-11-13 | ||
GB7939232 | 1979-11-13 | ||
GB8012789 | 1980-04-18 | ||
GB8012789 | 1980-04-18 | ||
GB8026420 | 1980-08-13 | ||
GB8026420 | 1980-08-13 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16006780A Division JPS56127346A (en) | 1979-11-13 | 1980-11-13 | Guanidine derivative, its manufacture and medicinal composition containing it and having gastric acid secretion inhibiting effect |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02191247A JPH02191247A (ja) | 1990-07-27 |
JPH0262547B2 true JPH0262547B2 (US06815460-20041109-C00097.png) | 1990-12-26 |
Family
ID=27260797
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1302281A Granted JPH02191247A (ja) | 1979-11-13 | 1989-11-22 | グアニジン誘導体 |
Country Status (15)
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ196923A (en) * | 1980-04-29 | 1983-12-16 | Shionogi & Co | 2-guanidino-4-(-acylaminoalkyl(thio)methyl)thiazoles and analogs |
DE3168031D1 (en) * | 1980-07-30 | 1985-02-14 | Ici Plc | Guanidine derivatives |
WO1982000462A1 (en) * | 1980-08-11 | 1982-02-18 | Rech Syntheses Organ | Imino-alkyl and amino-nitrile cyano-guanidines |
DE3270716D1 (en) * | 1981-02-27 | 1986-05-28 | Ici Plc | Guanidino-substituted heterocyclic derivatives having histamine h-2 antagonist activity |
CA1233818A (en) * | 1981-03-09 | 1988-03-08 | David J. Gilman | Guanidine derivatives as histamine h-2 receptor antagonists |
US4460584A (en) * | 1981-03-13 | 1984-07-17 | Imperial Chemical Industries Plc | Nitrogen heterocycles |
US4463005A (en) * | 1981-03-18 | 1984-07-31 | Imperial Chemical Industries Plc | Bicyclic guanidines |
IN158869B (US06815460-20041109-C00097.png) * | 1981-03-18 | 1987-02-07 | Ici Plc | |
EP0060730A3 (en) * | 1981-03-18 | 1982-12-08 | Imperial Chemical Industries Plc | Bicyclic derivatives |
US4451463A (en) * | 1981-03-24 | 1984-05-29 | Imperial Chemical Industries Plc | Alcohol derivatives |
EP0065823A1 (en) * | 1981-05-13 | 1982-12-01 | Imperial Chemical Industries Plc | Heterocyclic guanidines as histamine H-2 antagonists |
US4526973A (en) * | 1981-05-18 | 1985-07-02 | Bristol-Myers Company | Chemical compounds |
DE3267110D1 (de) * | 1981-05-18 | 1985-12-05 | Ici Plc | Amidine derivatives |
US4522943A (en) * | 1981-05-18 | 1985-06-11 | Bristol-Myers Company | Chemical compounds |
US4546188A (en) * | 1981-05-18 | 1985-10-08 | Bristol-Myers Company | Substituted 1,2-diaminocyclobutene-3,4-diones |
IE53068B1 (en) * | 1981-06-15 | 1988-05-25 | Merck & Co Inc | Diamino isothiazole-1-oxides and -1,1-dioxides as gastic secretion inhibitors |
FI832520L (fi) * | 1982-07-12 | 1984-01-13 | Bristol Myers Co | Farmaceutiska foerfaranden och sammansaettningar |
US4466965A (en) * | 1982-07-26 | 1984-08-21 | American Hospital Supply Corporation | Phthalazine compounds, compositions and use |
GR79384B (US06815460-20041109-C00097.png) * | 1982-08-20 | 1984-10-22 | Hoechst Uk Ltd | |
US4466970A (en) * | 1982-10-02 | 1984-08-21 | Smith Kline & French Laboratories Limited | Dioxocyclobutene compounds |
JPS5995281A (ja) * | 1982-11-19 | 1984-06-01 | Kotobuki Seiyaku Kk | チアゾ−ル誘導体及びその製造方法 |
JPS59104370A (ja) * | 1982-12-03 | 1984-06-16 | Kotobuki Seiyaku Kk | チアゾ−ル誘導体及びその製造方法 |
US4585781A (en) * | 1982-12-31 | 1986-04-29 | Glaxo Group Limited | Heterocyclic derivatives |
DE3334455A1 (de) * | 1983-03-04 | 1984-09-06 | Bayer Ag, 5090 Leverkusen | Guanidin - derivate |
JPS59167570A (ja) * | 1983-03-04 | 1984-09-21 | バイエル・アクチエンゲゼルシヤフト | グアニジン誘導体 |
ES521588A0 (es) * | 1983-03-30 | 1984-08-16 | Ferrer Int | Procedimiento de obtencion de nuevas n-ciano-formamidinas. |
US4567191A (en) * | 1983-06-07 | 1986-01-28 | Merck & Co., Inc. | Amino-phenyl-thiadiazoledioxides as gastric secretion inhibitors |
US4985459A (en) * | 1984-02-08 | 1991-01-15 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising diphenhydramine and methods of using same |
US4906625A (en) * | 1984-02-08 | 1990-03-06 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising diphenhydramine and metyhods of using same |
US4522826A (en) * | 1984-02-08 | 1985-06-11 | Richardson-Vicks Inc. | Analgesic and anti-inflammatory compositions comprising diphenhydramine and methods of using same |
US4683243A (en) * | 1984-02-08 | 1987-07-28 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising diphenhydramine and methods of using same |
US4755532A (en) * | 1984-02-08 | 1988-07-05 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising diphenhydramine and methods of using same |
US4560690A (en) * | 1984-04-30 | 1985-12-24 | Pfizer Inc. | 2-(N-substituted guanidino)-4-hetero-arylthiazole antiulcer agents |
GB8417194D0 (en) * | 1984-07-05 | 1984-08-08 | Boots Co Plc | Therapeutic agents |
KR890014504A (ko) * | 1988-03-11 | 1989-10-24 | 우대규 | 4-(2'-시아노 에틸티오)메틸-2-구아니디노티아졸의 제조방법 |
AU618355B2 (en) * | 1988-05-19 | 1991-12-19 | Hu-Metal Engineering Pty. Ltd. | Improvements relating to plate bending |
US5028716A (en) * | 1989-01-30 | 1991-07-02 | Taisho Pharmaceutical Co., Ltd. | 3,5-diamino-1,2,4-triazole derivatives |
FR2647112A1 (fr) * | 1989-05-22 | 1990-11-23 | Atochem | Composes polyfluoralkyle azotes, leurs procedes de preparation et leurs applications |
WO1994021621A1 (en) * | 1993-03-23 | 1994-09-29 | Astra Aktiebolag | Guanidine derivatives useful in therapy |
US6066740A (en) * | 1997-11-25 | 2000-05-23 | The Procter & Gamble Company | Process for making 2-amino-2-imidazoline, guanidine and 2-amino-3,4,5,6-tetrahydropyrimidine derivatives |
EP2725021A1 (de) | 2008-06-13 | 2014-04-30 | Bayer CropScience AG | Neue heteroaromatische Thioamide als Schädlingsbekämpfungsmittel |
EP2161259A1 (de) | 2008-09-03 | 2010-03-10 | Bayer CropScience AG | 4-Halogenalkylsubstituierte Diaminopyrimidine als Fungizide |
EP4196793A1 (en) | 2020-08-11 | 2023-06-21 | Université de Strasbourg | H2 blockers targeting liver macrophages for the prevention and treatment of liver disease and cancer |
USD1035780S1 (en) * | 2021-01-29 | 2024-07-16 | Fuzhou Leisiao Information Technology Co., Ltd. | Electric scooter |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4165378A (en) * | 1977-04-20 | 1979-08-21 | Ici Americas Inc. | Guanidine derivatives of imidazoles and thiazoles |
IE47044B1 (en) * | 1977-04-20 | 1983-12-14 | Ici Ltd | Guanidine derivatives |
GB2001624B (en) * | 1977-04-20 | 1982-03-03 | Ici Ltd | Guanidine derivatives processes for their manufacture and pharmaceutical compositions containing them |
EP0006679B1 (en) * | 1978-05-24 | 1982-07-21 | Imperial Chemical Industries Plc | Antisecretory thiadiazole derivatives, processes for their manufacture and pharmaceutical compositions containing them |
US4374836A (en) * | 1978-10-16 | 1983-02-22 | Imperial Chemical Industries Ltd. | Antisecretory heterocyclic derivatives, process for their manufacture and pharmaceutical compositions containing them |
EP0010893B1 (en) * | 1978-10-16 | 1984-02-08 | Imperial Chemical Industries Plc | Antisecretory branched-chain heterocyclic guanidine derivatives, processes for their manufacture, intermediates, and pharmaceutical compositions containing said derivatives |
US4200578A (en) * | 1978-12-18 | 1980-04-29 | Bristol-Myers Company | Thiazole derivatives |
JPS6056143B2 (ja) * | 1979-08-02 | 1985-12-09 | 山之内製薬株式会社 | アミジン誘導体ならびにその製造法 |
US4242351A (en) * | 1979-05-07 | 1980-12-30 | Imperial Chemical Industries Limited | Antisecretory oxadiazoles and pharmaceutical compositions containing them |
US4239908A (en) * | 1979-12-10 | 1980-12-16 | G.D. Searle & Co. | N-aralkenyl-N'-cyano-N"-(heterocyclylthioalkyl)-guanidines |
DE3270716D1 (en) * | 1981-02-27 | 1986-05-28 | Ici Plc | Guanidino-substituted heterocyclic derivatives having histamine h-2 antagonist activity |
US4451463A (en) * | 1981-03-24 | 1984-05-29 | Imperial Chemical Industries Plc | Alcohol derivatives |
US4336255A (en) * | 1981-03-24 | 1982-06-22 | Smithkline Corporation | Pharmaceutical compositions containing guanidinopyrimidines |
US4464378A (en) * | 1981-04-28 | 1984-08-07 | University Of Kentucky Research Foundation | Method of administering narcotic antagonists and analgesics and novel dosage forms containing same |
JPS59227870A (ja) * | 1983-06-07 | 1984-12-21 | Yamanouchi Pharmaceut Co Ltd | 新規2−グアニジノチアゾリン誘導体ならびにその製造法 |
-
1980
- 1980-11-07 GR GR63338A patent/GR71929B/el unknown
- 1980-11-11 DE DE8080304023T patent/DE3070127D1/de not_active Expired
- 1980-11-11 EP EP80304023A patent/EP0030092B1/en not_active Expired
- 1980-11-12 FI FI803540A patent/FI803540L/fi not_active Application Discontinuation
- 1980-11-12 US US06/206,005 patent/US4362728A/en not_active Expired - Lifetime
- 1980-11-12 NO NO803414A patent/NO803414L/no unknown
- 1980-11-12 CA CA000364482A patent/CA1136135A/en not_active Expired
- 1980-11-12 IL IL61468A patent/IL61468A0/xx unknown
- 1980-11-13 DK DK485080A patent/DK485080A/da unknown
- 1980-11-13 ES ES496810A patent/ES496810A0/es active Granted
- 1980-11-13 IE IE2359/80A patent/IE50440B1/en unknown
- 1980-11-13 PT PT72057A patent/PT72057B/pt unknown
- 1980-11-14 AU AU64420/80A patent/AU544314B2/en not_active Expired
- 1980-11-17 NZ NZ195568A patent/NZ195568A/xx unknown
-
1981
- 1981-11-30 ES ES507570A patent/ES507570A0/es active Granted
-
1982
- 1982-09-21 US US06/420,863 patent/US4604465A/en not_active Expired - Fee Related
-
1986
- 1986-06-02 US US06/869,615 patent/US4762932A/en not_active Expired - Fee Related
-
1989
- 1989-11-22 JP JP1302281A patent/JPH02191247A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
US4604465A (en) | 1986-08-05 |
ES8203076A1 (es) | 1982-03-01 |
DK485080A (da) | 1981-05-14 |
EP0030092A1 (en) | 1981-06-10 |
IL61468A0 (en) | 1980-12-31 |
IE50440B1 (en) | 1986-04-16 |
ES8207136A1 (es) | 1982-09-01 |
ES496810A0 (es) | 1982-03-01 |
AU544314B2 (en) | 1985-05-23 |
JPH02191247A (ja) | 1990-07-27 |
GR71929B (US06815460-20041109-C00097.png) | 1983-08-19 |
US4762932A (en) | 1988-08-09 |
AU6438480A (en) | 1981-09-17 |
EP0030092B1 (en) | 1985-02-06 |
NZ195568A (en) | 1983-04-12 |
ES507570A0 (es) | 1982-09-01 |
CA1136135A (en) | 1982-11-23 |
IE802359L (en) | 1981-05-13 |
US4362728A (en) | 1982-12-07 |
PT72057B (en) | 1981-09-24 |
NO803414L (no) | 1981-05-14 |
DE3070127D1 (en) | 1985-03-21 |
FI803540L (fi) | 1981-05-14 |
PT72057A (en) | 1980-12-01 |
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