Optically active 2-hydroxy tetrahydrothienopyridine derivatives, preparation method and use in manufacture of medicament thereof
Optically active 2-hydroxytetrahydrothienopyridine derivatives represented by Formula I and pharmaceutically acceptable salts, preparation method and use in the manufacture of a medicament thereof are disclosed. The pharmacodynamic experiment results show that the present compounds of Formula I are useful for inhibiting platelet aggregation. The pharmacokinetic experiment results show that the present compound of Formula I can be converted in vivo into pharmacologically active metabolites and are therefore useful for inhibiting platelet aggregation. Therefore, the present compounds are useful for the manufacture of a medicament for preventing or treating thrombosis and embolism related diseases.
1. A method for preparing an optically active 2-hydroxytetrahydro thienopyridine derivative, wherein said derivative is (S)-methyl 2-(2-acetoxy-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)-2-(2-chlorophenyl)-acetate of formula (I) or a pharmaceutically acceptable salt thereof, comprising the following steps:
(1) reacting an optically active compound of Formula II
with a compound of Formula III
or a salt thereof in the presence of a base, to obtain an optically active compound of Formula IV
or a salt thereof, wherein
R 7 is a C 1-6 alkyl, trifluoromethyl, pentafluoroethyl, heptafluoropropyl, phenyl, or a Z-substituted phenyl, in which Z is a C 1-3 alkyl, halo, cyano, nitro, or trifluoromethyl, and is at position 2, 3 or 4 of the phenyl ring; and
(2) reacting the compound of Formula IV or the salt thereof with a compound of Formula V
or a compound of Formula VI
in the presence of a base, to obtain the compound of Formula I,
2. A method for preparing an optically active 2-hydroxytetrahydro thienopyridine derivative, wherein said derivative is (S)-methyl 2-(2-acetoxy-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)-2-(2-chlorophenyl)-acetate of formula (I) or a pharmaceutically acceptable salt thereof, comprising the following step:
reacting an optically active compound of Formula II
with a compound of Formula VII
or a salt thereof in the presence of a base, to obtain the compound of Formula I,
wherein R 7 is a C 1-6 alkyl, trifluoromethyl, pentafluoroethyl, heptafluoropropyl, phenyl, or a Z-substituted phenyl, in which Z is a C 1-3 alkyl, halo, cyano, nitro, or trifluoromethyl, and is at position 2, 3 or 4 of the phenyl ring.
3. The method according to claim 1 , wherein in the step (1), a reaction solvent is used and is one or more selected from benzene, toluene, chloroform, n-hexane, cyclohexane, dichloromethane, 1,2-dichloroethane, methyl t-butyl ether, carbon tetrachloride, ethyl acetate, propyl acetate, butyl acetate, methanol, ethanol, acetone, tetrahydrofuran, diethyl ether, acetonitrile, N,N-dimethyl formamide, or dimethyl sulfoxide; the base used is selected from triethylamine, diisopropyl ethylamine, 1,8-diazabicyclo[5,4,0]undec-7-ene, potassium carbonate, sodium carbonate, potassium bicarbonate, or sodium bicarbonate; the reaction temperature is from −20° C. to 100° C.; and the salt of the compound of Formula III is selected from hydrochloride, p-toluenesulfonate, acetate, sulfate, phosphate, trifluoromethane sulfonate, oxalate, methanesulfonate, benzenesulfonate, or hydrobromide; and
wherein in the step (2), a reaction solvent is used and is one or more selected from benzene, toluene, chloroform, n-hexane, cyclohexane, dichloromethane, 1,2-dichloroethane, methyl t-butyl ether, carbon tetrachloride, ethyl acetate, propyl acetate, butyl acetate, methanol, ethanol, acetone, tetrahydrofuran, diethyl ether, acetonitrile, N,N-dimethyl formamide, or dimethyl sulfoxide; the base used is selected from triethylamine, sodium hydride, potassium hydride, 1,8-diazabicyclo[5,4,0]undec-7-ene, pyridine, diisopropylethylamine, lithium diisopropylamide, potassium carbonate, sodium carbonate, potassium bicarbonate, sodium bicarbonate, potassium t-butoxide, or sodium t-butoxide; and the reaction temperature is from −20° C. to 100° C.
4. The method according to claim 3 , wherein in the step (1), said reaction solvent is one or more selected from N,N-dimethyl formamide, tetrahydrofuran, acetonitrile, or dichloromethane; and said reaction temperature is from 10° C. to 60° C.
5. The method according to claim 3 , wherein in the step (2), said reaction solvent is one or more selected from tetrahydrofuran, acetonitrile, or N,N-dimethyl formamide; and said reaction temperature is from 0° C. to 50° C.
6. The method according to claim 2 , wherein a reaction solvent is used and is one or more selected from benzene, toluene, chloroform, n-hexane, cyclohexane, dichloromethane, 1,2-dichloroethane, methyl t-butyl ether, carbon tetrachloride, ethyl acetate, propyl acetate, butyl acetate, methanol, ethanol, acetone, tetrahydrofuran, diethyl ether, acetonitrile, N,N-dimethyl formamide, or dimethyl sulfoxide; the base used is selected from triethylamine, diisopropyl ethylamine, 1,8-diazabicyclo[5,4,0]undec-7-ene, potassium carbonate, sodium carbonate, potassium bicarbonate, or sodium bicarbonate; the reaction temperature is from −20° C. to 100° C.; and the salt of the compound of Formula VII is selected from hydrochloride, p-toluenesulfonate, acetate, sulfate, phosphate, trifluoromethane sulfonate, oxalate, methanesulfonate, benzenesulfonate, or hydrobromide.
7. The method according to claim 6 , wherein said solvent is one or more selected from N,N-dimethyl formamide, tetrahydrofuran, acetonitrile, or dichloromethane; and the reaction temperature is from 10° C. to 60° C.
8. A method for preparing an optically active 2-hydroxytetrahydro thienopyridine derivative, wherein said derivative is (S)-methyl 2-(2-acetoxy-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)-2-(2-chlorophenyl)-acetate of formula (I) or a pharmaceutically acceptable salt thereof, comprising the following step:
reacting the optically active compound of Formula IV
or the salt thereof with a compound of Formula V
or a compound of Formula VI
in the presence of a base, to obtain the compound of Formula I,
9. The method according to claim 8 , wherein a reaction solvent is used and is one or more selected from benzene, toluene, chloroform, n-hexane, cyclohexane, dichloromethane, 1,2-dichloroethane, methyl t-butyl ether, carbon tetrachloride, ethyl acetate, propyl acetate, butyl acetate, methanol, ethanol, acetone, tetrahydrofuran, diethyl ether, acetonitrile, N,N-dimethyl formamide, or dimethyl sulfoxide; the base used is selected from triethylamine, sodium hydride, potassium hydride, 1,8-diazabicyclo[5,4,0]undec-7-ene, pyridine, diisopropylethylamine, lithium diisopropylamide, potassium carbonate, sodium carbonate, potassium bicarbonate, sodium bicarbonate, potassium t-butoxide, or sodium t-butoxide; and the reaction temperature is from −20° C. to 100° C.