【结 构 式】 |
【分子编号】61051 【品名】ethyl 2-pyrrolidinecarboxylate 【CA登记号】 |
【 分 子 式 】C5H9NO2 【 分 子 量 】115.132 【元素组成】C 52.16% H 7.88% N 12.17% O 27.79% |
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 esterification of proline (I) with SOCl2 and ethanol gives ethyl prolinate (II), which by treatment with NH3 in methanol is converted into prolinamide (III). The acylation of (III) with cyclopropylcarbonyl chloride (IV) by means of K2CO3 in acetone yields 1-cyclopropylcarbonyl-2-carbamoylpyrrolidine (V), which is reduced with LiAlH4 in ether to afford 1-cyclopropylmethyl-2-aminomethylpyrrolidine (VI) (1,2). Finally this compound is condensed with ethyl 5-sulfamoyl-2-methoxybenzoate (VII) by heating at 120 C
【1】 Kaplan, J.P.; et al. (Synthelabo, S.A.); BE 857544; DE 2735036; FR 2360572; FR 2372157; FR 2395261; GB 1555890; JP 7825563; NL 7708571; ZA 7704743 . |
【2】 Kaplan, J.P.; et al. (Synthelabo, S.A.); BE 836752; CA 1039731; CH 612668; DE 2556457; FR 2294698; FR 2327771; FR 2331345; GB 1508880; JP 7748661; NL 7514620; US 4021567; US 4156060; US 4172143; US 4189495; ZA 7507828 . |
【3】 (Synthelabo, S.A.); BE 861866; FR 2394529; GB 1560019; JP 7905969; NL 7713631; ZA 7706950 . |
【4】 Blancafort, P.; Serradell, M.N.; Castaner, J.; Hillier, K.; Cipropride. Drugs Fut 1981, 6, 4, 220. |
【5】 Obitz, D.C.L. (Synthelabo, S.A.); FR 2393794 . |
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) | 61051 | ethyl 2-pyrrolidinecarboxylate | C5H9NO2 | 详情 | 详情 | |
(II) | 61052 | ethyl 2-pyrrolidinecarboxylate | C7H13NO2 | 详情 | 详情 | |
(III) | 22654 | 2-pyrrolidinecarboxamide | 2812-47-7 | C5H10N2O | 详情 | 详情 |
(IV) | 14601 | N-(2-oxo-2-phenylethyl)acetamide | C10H11NO2 | 详情 | 详情 | |
(V) | 61053 | 1-(cyclopropylcarbonyl)-2-pyrrolidinecarboxamide | C9H14N2O2 | 详情 | 详情 | |
(VI) | 61054 | [1-(cyclopropylmethyl)-2-pyrrolidinyl]methanamine; [1-(cyclopropylmethyl)-2-pyrrolidinyl]methylamine | C9H18N2 | 详情 | 详情 | |
(VII) | 61055 | ethyl 5-(aminosulfonyl)-2-methoxybenzoate | C10H13NO5S | 详情 | 详情 |
Extended Information