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【结 构 式】

【分子编号】21335

【品名】ethyl 2-[[2-(4-chlorophenyl)-4-methyl-1,3-oxazol-5-yl]methoxy]-2-methylpropanoate

【CA登记号】

【 分 子 式 】C17H20ClNO4

【 分 子 量 】337.80284

【元素组成】C 60.45% H 5.97% Cl 10.5% N 4.15% O 18.95%

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:(VI)

Romazarit (sodium salt) is prepared by a 7-step process from 4-chlorobenzoic acid, ethyl 2-chloroacetoacetate (VIII) and ethyl 2-methyl 2-hydroxypropionate (X). Reaction of the sodium salt of 4-chlorobenzoic acid (I) with ethyl 2-chloroacetoacetate (VIII) affords ethyl 3-oxo-2-(4-chlorophenylcarboxy)butyrate (II). Cyclization of (II) to ethyl 2-(4-chlorophenyl)-4-methyloxazole-5-carboxylate (III) is accomplished by treatment with formamide (IX)/sulfuric acid. Reduction of the ester (III) with lithium aluminum hydroxide in tetrahydrofuran yields 2-(4-chlorophenyl)-4-methyl-5-oxazolemethanol (IV). Chlorination of alcohol (IV) with thionyl chloride followed by reaction of crude chloromethyloxazole (V) with the sodium alkoxide derivative of ethyl 2-methyl-2-hydroxypropionate (X) yields ethyl [2-[(4-chlorophenyl)-4-methyl-5-oxazolyl]methoxy]-2-methylpropionate (VI). Hydrolysis of the ester (VI), acidification and recrystallization affords Ro 31-3948 (VII) as a white solid, which is converted to the sodium salt by treatment with sodium isopropoxide in isopropanol.

1 Self, C.R.; Machin, P.J.; Osbond, J.M.; Smithen, C.E.; Tong, B.P. (Hoffmann-La Roche, Inc.); Oxazole and isoxazole derivatives having anti-arthritic activity.. EP 0220573; ES 2002420; ES 2010537; US 4774253 .
2 Bradshaw, D.; Sedgwick, A.D.; Self, C.R.; ROMAZARIT SODIUM < Prop INNM; BAN >. Drugs Fut 1989, 14, 9, 867.
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) 18359 p-chlorobenzoic acid; 4-chlorobenzoic acid 74-11-3 C7H5ClO2 详情 详情
(II) 21331 1-(ethoxycarbonyl)-2-oxopropyl 4-chlorobenzoate C13H13ClO5 详情 详情
(III) 21332 ethyl 2-(4-chlorophenyl)-4-methyl-1,3-oxazole-5-carboxylate C13H12ClNO3 详情 详情
(IV) 13450 [2-(4-Chlorophenyl)-4-methyl-1,3-oxazol-5-yl]methanol C11H10ClNO2 详情 详情
(V) 21334 5-(chloromethyl)-2-(4-chlorophenyl)-4-methyl-1,3-oxazole C11H9Cl2NO 详情 详情
(VI) 21335 ethyl 2-[[2-(4-chlorophenyl)-4-methyl-1,3-oxazol-5-yl]methoxy]-2-methylpropanoate C17H20ClNO4 详情 详情
(VII) 21336 2-[[2-(4-chlorophenyl)-4-methyl-1,3-oxazol-5-yl]methoxy]-2-methylpropionic acid C15H16ClNO4 详情 详情
(VIII) 21337 ethyl 2-chloro-3-oxobutanoate 609-15-4 C6H9ClO3 详情 详情
(IX) 16595 4-nitrophenyl 1,3-thiazol-5-ylmethyl carbonate 144163-97-3 C11H8N2O5S 详情 详情
(X) 21339 ethyl 2-hydroxy-2-methylpropanoate 80-55-7 C6H12O3 详情 详情
Extended Information