홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ethyl-alpha-carbethoxy-4-methylamino-2-nitrodihydrocinnamate → 7-Methylamino-3-carbethoxy-3,4-dihydro-2-quinolone

HRID 637760
노트
인쇄 미리보기

반응식

HRID 637760 반응식
[CH2:1]([O:3][C:4](=[O:23])[CH:5]([C:18](OCC)=[O:19])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][CH3:14])=[CH:9][C:8]=1[N+:15]([O-])=O)[CH3:2].[H][H]>[Pd].O1CCOCC1>[CH3:14][NH:13][C:10]1[CH:9]=[C:8]2[C:7]([CH2:6][CH:5]([C:4]([O:3][CH2:1][CH3:2])=[O:23])[C:18](=[O:19])[NH:15]2)=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21280186Ethyl-alpha-carbethoxy-4-methylamino-2-nitrodihydrocinnamateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 212801857-Methylamino-3-carbethoxy-3,4-dihydro-2-quinolone수율 25.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 312751,4-Dioxane용매

실험 절차

A mixture of 2.6 g of the diester (4), of 10% Pd on charcoal and 75 mL of dioxane were shaken under 50 psi of hydrogen for 17 hours at 50° C. The catalyst was removed by filtering through Celite and the solvent was removed. The residue was chromatographed on 200 g of silica gel eluting with 3:17 (v/v) acetone: CH2Cl2. Fractions 75-120 (17 mL/fraction) were combined and concentrated to yield 0.5 g of a white powder. Recrystallization from MeOH-H2O produced an analytical sample, m.p. 171°-172° C.

후처리

  1. customThe catalyst was removed
  2. filtrationby filtering through Celite
  3. customthe solvent was removed
  4. customThe residue was chromatographed on 200 g of silica gel eluting with 3:17 (v/v) acetone
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-05eaea8941df441782cce78a6d1a6cc1
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04558130

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트