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

2-Nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile → 2-Amino-5-(3-oxo-morpholin-4-YL)-benzonitrile

HRID 2244683
노트
인쇄 미리보기

반응식

HRID 2244683 반응식
[N+:1]([C:4]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][C:13]2=[O:18])=[CH:8][C:5]=1[C:6]#[N:7])([O-])=O>C1COCC1.[Pd]>[NH2:1][C:4]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][C:13]2=[O:18])=[CH:8][C:5]=1[C:6]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 588264662-Nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile

생성물 1

HCID 534164642-Amino-5-(3-oxo-morpholin-4-YL)-benzonitrile수율 60%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-nitro-5-(3-oxo-morpholin-4-yl)-benzonitrile (1.1 g) in THF (80 ml) was hydrogenated at 1 atm in the presence of Pd/C 10% (350 mg) at room temperature. The reaction mixture was filtered through decalite and precipitated (AcOEt/heptane) to yield 2-amino-5-(3-oxo-morpholin-4-yl)-benzonitrile as a white solid (580 mg). MS: 218.4 ([M+H]+).

후처리

  1. filtrationThe reaction mixture was filtered through decalite
  2. customprecipitated (AcOEt/heptane)

출처 및 근거

ORD 기록
ord-435057e56a614cf9996b8dedd617d7d3
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07678917B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트