UA118755C2 - Похідне дигідропіридазин-3,5-діону - Google Patents

Info

Publication number

UA118755C2

UA118755C2 UAA201509770A UAA201509770A UA118755C2 UA 118755 C2 UA118755 C2 UA 118755C2 UA A201509770 A UAA201509770 A UA A201509770A UA A201509770 A UAA201509770 A UA A201509770A UA 118755 C2 UA118755 C2 UA 118755C2

Authority

UA

Ukraine

Prior art keywords

optionally substituted

methyl

alkyl

substituents

trifluoromethyl

Prior art date

2013-03-13

Links

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• Global Dossier
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• 150000001875 compounds Chemical class 0.000 claims abstract description 621
• 150000003839 salts Chemical class 0.000 claims abstract description 337
• 201000005991 hyperphosphatemia Diseases 0.000 claims abstract description 25
• 239000003814 drug Substances 0.000 claims abstract description 19
• 230000000069 prophylactic effect Effects 0.000 claims abstract description 12
• 229940124597 therapeutic agent Drugs 0.000 claims abstract description 12
• 239000004480 active ingredient Substances 0.000 claims abstract description 10
• 125000000217 alkyl group Chemical group 0.000 claims description 461
• -1 (ethoxy)carbonyl Chemical group 0.000 claims description 436
• 125000001424 substituent group Chemical group 0.000 claims description 424
• 125000005843 halogen group Chemical group 0.000 claims description 302
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 190
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 186
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 139
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 126
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 111
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 73
• 125000004076 pyridyl group Chemical group 0.000 claims description 72
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 64
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 48
• 229910052757 nitrogen Inorganic materials 0.000 claims description 48
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 48
• 125000004043 oxo group Chemical group O=* 0.000 claims description 43
• 229910052799 carbon Inorganic materials 0.000 claims description 41
• 125000002757 morpholinyl group Chemical group 0.000 claims description 41
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 40
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 39
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 35
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 27
• 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 26
• 125000002837 carbocyclic group Chemical group 0.000 claims description 23
• 125000004432 carbon atom Chemical group C* 0.000 claims description 21
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 20
• 239000002253 acid Substances 0.000 claims description 19
• 208000020832 chronic kidney disease Diseases 0.000 claims description 19
• 229910052736 halogen Inorganic materials 0.000 claims description 19
• 208000005770 Secondary Hyperparathyroidism Diseases 0.000 claims description 18
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 17
• 208000022831 chronic renal failure syndrome Diseases 0.000 claims description 17
• 125000003386 piperidinyl group Chemical group 0.000 claims description 17
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
• 150000002367 halogens Chemical class 0.000 claims description 16
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 16
• 125000004193 piperazinyl group Chemical group 0.000 claims description 15
• 229910052731 fluorine Inorganic materials 0.000 claims description 13
• 125000001544 thienyl group Chemical group 0.000 claims description 12
• 201000010099 disease Diseases 0.000 claims description 11
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
• 125000001153 fluoro group Chemical group F* 0.000 claims description 10
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 10
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 9
• 125000002393 azetidinyl group Chemical group 0.000 claims description 9
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 9
• 239000003795 chemical substances by application Substances 0.000 claims description 8
• 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 8
• 229910052801 chlorine Inorganic materials 0.000 claims description 7
• 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 7
• 125000002541 furyl group Chemical group 0.000 claims description 7
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 6
• 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 6
• 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 6
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
• FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 4
• 239000000460 chlorine Chemical group 0.000 claims description 4
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
• CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 claims description 4
• JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 4
• 125000001041 indolyl group Chemical group 0.000 claims description 4
• CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
• 238000011161 development Methods 0.000 claims description 3
• 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
• 125000001425 triazolyl group Chemical group 0.000 claims description 3
• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
• NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 3
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
• WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 2
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
• GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 claims description 2
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
• FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
• 239000011737 fluorine Substances 0.000 claims 4
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
• 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 2
• MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 claims 2
• KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
• GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
• 229960005137 succinic acid Drugs 0.000 claims 1
• 239000012453 solvate Substances 0.000 abstract description 313
• 238000000034 method Methods 0.000 abstract description 80
• 239000003112 inhibitor Substances 0.000 abstract description 17
• 239000011734 sodium Substances 0.000 abstract description 14
• 229910052708 sodium Inorganic materials 0.000 abstract description 14
• 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 abstract description 11
• 230000002265 prevention Effects 0.000 abstract description 10
• 108010092528 Phosphate Transport Proteins Proteins 0.000 abstract description 8
• 102000016462 Phosphate Transport Proteins Human genes 0.000 abstract description 8
• 230000001419 dependent effect Effects 0.000 abstract description 8
• 229940079593 drug Drugs 0.000 abstract description 7
• 239000008194 pharmaceutical composition Substances 0.000 abstract description 6
• 125000003545 alkoxy group Chemical group 0.000 description 341
• 125000000592 heterocycloalkyl group Chemical group 0.000 description 207
• 125000000304 alkynyl group Chemical group 0.000 description 112
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 111
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 109
• 125000003118 aryl group Chemical group 0.000 description 77
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 63
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 58
• 238000006243 chemical reaction Methods 0.000 description 52
• 239000000203 mixture Substances 0.000 description 51
• 125000001313 C5-C10 heteroaryl group Chemical group 0.000 description 50
• 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 47
• 125000004414 alkyl thio group Chemical group 0.000 description 42
• 239000002904 solvent Substances 0.000 description 40
• 150000001721 carbon Chemical group 0.000 description 38
• 125000000623 heterocyclic group Chemical group 0.000 description 37
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 36
• 239000011541 reaction mixture Substances 0.000 description 35
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 32
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 32
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 32
• 125000005842 heteroatom Chemical group 0.000 description 31
• 239000000243 solution Substances 0.000 description 31
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 28
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 28
• 125000000753 cycloalkyl group Chemical group 0.000 description 28
• 239000012634 fragment Substances 0.000 description 28
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 27
• 239000012044 organic layer Substances 0.000 description 27
• 229910052698 phosphorus Inorganic materials 0.000 description 26
• 238000004128 high performance liquid chromatography Methods 0.000 description 25
• OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 24
• OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 24
• 239000011574 phosphorus Substances 0.000 description 24
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 24
• 230000002829 reductive effect Effects 0.000 description 24
• 150000003857 carboxamides Chemical class 0.000 description 23
• 239000012043 crude product Substances 0.000 description 23
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 23
• 125000001072 heteroaryl group Chemical group 0.000 description 23
• 125000004178 (C1-C4) alkyl group Chemical class 0.000 description 22
• 238000007429 general method Methods 0.000 description 21
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 20
• 125000004429 atom Chemical group 0.000 description 20
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 19
• 238000004587 chromatography analysis Methods 0.000 description 19
• 238000002425 crystallisation Methods 0.000 description 19
• 230000008025 crystallization Effects 0.000 description 19
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
• 125000002252 acyl group Chemical group 0.000 description 18
• DNMZJIGSDQVGSA-UHFFFAOYSA-N methoxymethane;hydrochloride Chemical compound Cl.COC DNMZJIGSDQVGSA-UHFFFAOYSA-N 0.000 description 18
• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 18
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 17
• 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 description 17
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 16
• 125000004430 oxygen atom Chemical group O* 0.000 description 16
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 16
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
• 239000002585 base Substances 0.000 description 14
• 239000003153 chemical reaction reagent Substances 0.000 description 14
• 230000014759 maintenance of location Effects 0.000 description 14
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
• 125000003277 amino group Chemical group 0.000 description 12
• 229910000027 potassium carbonate Inorganic materials 0.000 description 12
• 229920006395 saturated elastomer Polymers 0.000 description 12
• 125000004568 thiomorpholinyl group Chemical group 0.000 description 12
• PIKNVEVCWAAOMJ-UHFFFAOYSA-N 3-fluorobenzaldehyde Chemical compound FC1=CC=CC(C=O)=C1 PIKNVEVCWAAOMJ-UHFFFAOYSA-N 0.000 description 11
• LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 11
• 239000003463 adsorbent Substances 0.000 description 11
• 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 11
• 239000007864 aqueous solution Substances 0.000 description 11
• 125000004212 difluorophenyl group Chemical group 0.000 description 11
• 239000007788 liquid Substances 0.000 description 11
• DMYLUKNFEYWGCH-UHFFFAOYSA-N pyridazine-3-carboxamide Chemical compound NC(=O)C1=CC=CN=N1 DMYLUKNFEYWGCH-UHFFFAOYSA-N 0.000 description 11
• 239000011780 sodium chloride Substances 0.000 description 11
• 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 11
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 10
• ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical compound OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 10
• 125000003282 alkyl amino group Chemical group 0.000 description 10
• 238000009835 boiling Methods 0.000 description 10
• 238000000605 extraction Methods 0.000 description 10
• 125000001207 fluorophenyl group Chemical group 0.000 description 10
• 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 10
• 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 9
• KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 9
• 150000001412 amines Chemical class 0.000 description 9
• 230000015572 biosynthetic process Effects 0.000 description 9
• FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 9
• 229910000024 caesium carbonate Inorganic materials 0.000 description 9
• 230000002401 inhibitory effect Effects 0.000 description 9
• 239000012299 nitrogen atmosphere Substances 0.000 description 9
• 125000003566 oxetanyl group Chemical group 0.000 description 9
• 125000000168 pyrrolyl group Chemical group 0.000 description 9
• 239000012312 sodium hydride Substances 0.000 description 9
• 229910000104 sodium hydride Inorganic materials 0.000 description 9
• 239000007858 starting material Substances 0.000 description 9
• 229910052717 sulfur Inorganic materials 0.000 description 9
• 125000004434 sulfur atom Chemical group 0.000 description 9
• 238000003786 synthesis reaction Methods 0.000 description 9
• SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 8
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
• 238000010521 absorption reaction Methods 0.000 description 8
• 238000004458 analytical method Methods 0.000 description 8
• 125000002619 bicyclic group Chemical group 0.000 description 8
• 239000003054 catalyst Substances 0.000 description 8
• 238000004440 column chromatography Methods 0.000 description 8
• 239000000741 silica gel Substances 0.000 description 8
• 229910002027 silica gel Inorganic materials 0.000 description 8
• 229910052938 sodium sulfate Inorganic materials 0.000 description 8
• 235000011152 sodium sulphate Nutrition 0.000 description 8
• 230000009466 transformation Effects 0.000 description 8
• LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 8
• 238000005160 1H NMR spectroscopy Methods 0.000 description 7
• 125000002950 monocyclic group Chemical group 0.000 description 7
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 7
• 238000002360 preparation method Methods 0.000 description 7
• 229940002612 prodrug Drugs 0.000 description 7
• 239000000651 prodrug Substances 0.000 description 7
• 125000001412 tetrahydropyranyl group Chemical group 0.000 description 7
• 238000000844 transformation Methods 0.000 description 7
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 6
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
• RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 6
• XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 6
• 235000011054 acetic acid Nutrition 0.000 description 6
• HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 6
• 210000004369 blood Anatomy 0.000 description 6
• 239000008280 blood Substances 0.000 description 6
• 239000011575 calcium Substances 0.000 description 6
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
• ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 6
• 229910000396 dipotassium phosphate Inorganic materials 0.000 description 6
• 235000019797 dipotassium phosphate Nutrition 0.000 description 6
• 125000001033 ether group Chemical group 0.000 description 6
• 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 6
• 210000001035 gastrointestinal tract Anatomy 0.000 description 6
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
• NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
• LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
• RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
• WDBAXYQUOZDFOJ-UHFFFAOYSA-N 2,3-difluorobenzaldehyde Chemical compound FC1=CC=CC(C=O)=C1F WDBAXYQUOZDFOJ-UHFFFAOYSA-N 0.000 description 5
• 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 5
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 5
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 5
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
• AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 5
• 125000003342 alkenyl group Chemical group 0.000 description 5
• 125000002947 alkylene group Chemical group 0.000 description 5
• 150000001408 amides Chemical group 0.000 description 5
• 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
• 239000012267 brine Substances 0.000 description 5
• 229940126601 medicinal product Drugs 0.000 description 5
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