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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620284생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Methoxy-1-butanolHCID 17291—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물o-Desmethyl metoclopramideHCID 9817332—
용매TetrahydrofuranHCID 8028—
생성물4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(3-methoxy-butoxy)-benzamideHCID 992937652.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04820715
출처 데이터셋uspto-grants-1989_04
ORD IDord-56c9973285944906806d04864c153888
출처 메모uspto-grants-1989_04