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【结 构 式】

【分子编号】38042

【品名】(3R,4R)-4-(3-acetyl-2-hydroxy-4,6-dimethoxyphenyl)-1-methylpiperidinyl acetate

【CA登记号】

【 分 子 式 】C18H25NO6

【 分 子 量 】351.39964

【元素组成】C 61.52% H 7.17% N 3.99% O 27.32%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

The condensation of acetophenone (I) with 2-chlorobenzoyl chloride (II) in pyridine gives the corresponding ester (III), which is treated with KOH in hot pyridine yielding the diketone (IV). The cyclization of (IV) with H2SO4 in acetic acid at 100 C affords the benzopyranone (V). The hydrolysis of the acetate group of (V) with NaOH in methanol/water affords the piperidinol (VI), which is finally demethylated with pyridinium hydrochloride at 210-20 C. Alternatively, the ester (III) can be cyclized directly to benzopyranone (V) by means of NaH in hot dioxane.

1 Naik, R.G.; Lal, B.; Rupp, R.H.; Sedlacek, H.H.; Dickneite, G.; Czech, J. (Aventis SA); Use of 4H-1-benzopyran-4-one derivs., 4H-1-benzopyran-4-one derivs. and medicines containing same. AU 8943841; DE 3836676; EP 0366061; JP 1990178225; US 5284856 .
2 Tabaka, A.C.; et al.; Application of modified flavone closure for the preparation of racemic L86-8275. Org Process Res Dev 1999, 3, 4, 256.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 38042 (3R,4R)-4-(3-acetyl-2-hydroxy-4,6-dimethoxyphenyl)-1-methylpiperidinyl acetate C18H25NO6 详情 详情
(II) 14000 o-Chlorobenzoyl chloride; 2-Chlorobenzoyl chloride 609-65-4 C7H4Cl2O 详情 详情
(III) 38043 2-acetyl-6-[(3R,4R)-3-(acetoxy)-1-methylpiperidinyl]-3,5-dimethoxyphenyl 2-chlorobenzoate C25H28ClNO7 详情 详情
(IV) 38044 (3R,4R)-4-[3-[3-(2-chlorophenyl)-3-oxopropanoyl]-2-hydroxy-4,6-dimethoxyphenyl]-1-methylpiperidinyl acetate C25H28ClNO7 详情 详情
(V) 38045 (3R,4R)-4-[2-(2-chlorophenyl)-5,7-dimethoxy-4-oxo-4H-chromen-8-yl]-1-methylpiperidinyl acetate C25H26ClNO6 详情 详情
(VI) 38046 2-(2-chlorophenyl)-8-[(3R,4R)-3-hydroxy-1-methylpiperidinyl]-5,7-dimethoxy-4H-chromen-4-one C23H24ClNO5 详情 详情
Extended Information