反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Mix 6-[4-(azetidin-3-yloxy)-3-methoxy-phenyl]-2-(4-chloro-phenyl)-6H-thieno[2,3-c]pyridin-7-one trifluoroacetic acid salt (210 mg, 0.48 mmol) with methanol (10 mL) and acetic acid (0.3 mL). Add a solution of formaldehyde (0.20 mL, 2.66 mmol, 37% aqueous solution) and stir the mixture for 15 min. Add sodium cyanoborohydride (110 mg, 1.75 mmol) and stir the mixture at RT overnight. Concentrate the mixture in vacuo and partition the crude material between saturated NaHCO3 (25 mL) and CH2Cl2 (25 mL). Remove the organic solution and extract the aqueous phase with additional CH2Cl2 (2×25 mL). Combine the organic solutions and concentrate in vacuo. Purify the crude material by flash chromatography, using 5% MeOH (2N NH3) in CH2Cl2 as eluent, to give 133 mg (61%) of 2-(4-chloro-phenyl)-6-[3-methoxy-4-(1-methyl-azetidin-3-yloxy)-phenyl]-6H-thieno[2,3-c]pyridin-7-one as a white solid.
WORKUP
后处理
- concentrationConcentrate the mixture in vacuo
- custompartition the crude material between saturated NaHCO3 (25 mL) and CH2Cl2 (25 mL)
- customRemove the organic solution
- extractionextract the aqueous phase with additional CH2Cl2 (2×25 mL)
- concentrationCombine the organic solutions and concentrate in vacuo
- customPurify the crude material by flash chromatography