Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620266생성일: 2026년 10월 24일
o-Desmethyl metoclopramide → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamide
https://huagongshe.com/ko/reaction/620266
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | o-Desmethyl metoclopramide | HCID 9817332 | — |
| 반응물 | 3-Bromo-2-pentanone | HCID 10012249 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamide | HCID 14116894 | 20.3% |
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 Prepration 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 ether--petroleum ether to yield 1.5 g of the title compound, mp. 75°-78°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ 8.26 (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, 6H); 2.1 (s, 3H); 2.1-1.7 (m, 2H); 1.05 (m, 9H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04820715 |
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| 출처 데이터셋 | uspto-grants-1989_04 |
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| ORD ID | ord-a97e27bc5770454fa7262d9d3cf79a65 |
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| 출처 메모 | uspto-grants-1989_04 |
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