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【结 构 式】

【分子编号】31972

【品名】4-[2-(benzoylamino)-3-(dipropylamino)-3-oxopropyl]phenyl benzoate

【CA登记号】

【 分 子 式 】C29H32N2O4

【 分 子 量 】472.58416

【元素组成】C 73.71% H 6.83% N 5.93% O 13.54%

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:(IV)

The benzoylation of tyrosine (I) with benzoyl chloride (II) in aqueous NaOH gives O,N-(di-benzoyl)-D,L-tyrosine (III), which by reaction with di-n-propylamine (A) by means of ethyl chlorocarbonate and triethylamine in acetone is converted into O,N-(di-benzoyl)-D,L-tyrosyl-di-n-propylamide (IV). Selective hydrolysis of (IV) with NaOH in methanol - water affords N-benzoyl-D,L-tyrosyl-di-n-propylamide (V), which is finally condensed with 2-(diethylamino)ethyl chloride (VI) by means of sodium methoxide in refluxing toluene.

1 Senin; et al.; Activity of derivatives of tyrosine on gastrointestinal motility. Gastrointestinal Motility in Health and Disease. Duthie, H.L. (Ed.); MTP Press Limited, Lancaster 1978, 417-427.
2 Makovec, F.; Rovati, L.; Senini, P. (Rotta Research Laboratorium SpA); O-Tertiary amino-alkyl-N-benzoyl tyrosil amides. DE 2503992; FR 2259592; GB 1467927; JP 50116442; NL 167683C; US 4004008 .
3 Serradell, M.N.; de Angelis, L.; Blancafort, P.; Castaner, J.; Tiropramide. Drugs Fut 1982, 7, 6, 413.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 21856 N,N-dipropylamine; N-propyl-1-propanamine 142-84-7 C6H15N 详情 详情
(I) 31970 4-Hydroxy-17O-phenylalanine; Hydroxy Phenyl Alanine; DL-tyrosine; 2-Amino-3-(4-hydroxyphenyl)propionic acid; 3-(4-Hydroxyphenyl)alanine; beta-(p-Hydroxyphenyl)alanine; tyrosine 556-03-6 C9H11NO3 详情 详情
(II) 10463 Benzoyl chloride 98-88-4 C7H5ClO 详情 详情
(III) 31971 N-benzoyl-4-(benzoyloxy)phenylalanine C23H19NO5 详情 详情
(IV) 31972 4-[2-(benzoylamino)-3-(dipropylamino)-3-oxopropyl]phenyl benzoate C29H32N2O4 详情 详情
(V) 31973 N-[2-(dipropylamino)-1-(4-hydroxybenzyl)-2-oxoethyl]benzamide C22H28N2O3 详情 详情
(VI) 16194 2-chloro-N,N-diethyl-1-ethanamine; N-(2-chloroethyl)-N,N-diethylamine 100-35-6 C6H14ClN 详情 详情
Extended Information