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HRID 620284作成日:2026年10月24日

Triphenylphosphine → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(3-methoxy-butoxy)-benzamide

https://huagongshe.com/ja/reaction/620284

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Methoxy-1-butanolHCID 17291—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物o-Desmethyl metoclopramideHCID 9817332—
溶媒TetrahydrofuranHCID 8028—
生成物4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(3-methoxy-butoxy)-benzamideHCID 992937652.4%

反応手順

A stirred solution of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (1.715 g, 6 mmoles; prepared according to Preparation 1B), triphenylphosphine (1.58 g, 6 mmoles), 3-methoxy-1-butanol (0.62 g, 6 mmoles) in dry tetrahydrofuran (50 ml) was treated dropwise with diethyl azodicarboxylate (1.1 g of 95% purity material, 6 mmoles). The solution was left to stir overnight. After evaporation of the solvent the residue was dissolved in methylene chloride. The solution was washed with 0.4N NaOH, water, dried and the solvent evaporated. The residue was chromatographed over deactivated silica using methylene chloride (100), methanol (2.5), ammonium hydroxide (0.5) solvent system. The appropriate fractions were combined and the solvent evaporated. The residue (1.7 g) was crystallized from toluene to yield 1.17 g (52%) of the title compound, m.p. 76°-78° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04820715
出典データセットuspto-grants-1989_04
ORD IDord-56c9973285944906806d04864c153888
出典メモuspto-grants-1989_04