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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1382965생성일: 2026년 10월 26일

o-Desmethyl metoclopramide → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamide

https://huagongshe.com/reaction/1382965

반응식

참여 물질

역할이름HCID투입량
반응물o-Desmethyl metoclopramideHCID 9817332—
반응물3-Bromo-2-pentanoneHCID 10012249—
용매AcetonitrileHCID 6342—
생성물4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamideHCID 1411689420.3%

반응 단계

A solution of the tetrabutylammonium salt of 4-amino-5- chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (10.5 g, 20 mmoles) (from Preparation No. 3) in acetonitrile (150 ml) was treated with 3-bromo-2-pentanone (3.3 g of 80%, 20 mmoles, contaminated with 15% of 1-bromo-2-pentanone) [obtained according to the procedure of E. T. Borrows, D. O. Holland and J. Kenyon, J. Chem. Soc. 1083, (1946)]. After 3 hours, the solvent was evaporated and the residue partitioned between ethyl acetate and water. The organic phase was washed with water, dried, and the solvent evaporated. The semisolid residue was triturated with ether to yield a solid which was recrystallized from etherpetroleum ether to yield 1.5 g of the title compound, mp. 75°-78°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ8.26 (s, 1H); 8.14 (bs, 1H); 6.1 (s, 1H); 4.5 (t, 1H); 4.4 (s, 2H); 3.69 (q, 2H); 2.64 (m, 6 H); 2.1 (s, 3H); 2.1-1.7 (m, 2H); 1.05 (m, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04808624
출처 데이터셋uspto-grants-1989_02
ORD IDord-e66f7f589b6d4e17bb90f44fa34a51a3
출처 메모uspto-grants-1989_02