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

HCID 68838102, 화합물 → HCID 68835059, 화합물

HRID 490562
노트
인쇄 미리보기

반응식

HRID 490562 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH2:13][CH2:14][C:15]#[N:16])[NH:8][C:7]2=[O:17])([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH2:13][CH2:14][C:15]#[N:16])[NH:8][C:7]2=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68838102HCID 68838102, 화합물

생성물 1

HCID 68835059HCID 68835059, 화합물수율 99.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 3-(5-Nitro-3-oxo-2,3-dihydro-indazol-1-yl)-propionitrile (0.521 g) in MeOH (50 mL) was added Pd/C(10%) catalyst (0.13 g) and the reaction mixture was stirred for 20 hours at ambient temperature under a hydrogen atmosphere using a balloon. After this time the reaction mixture was filtered through Celite® which was washed with more EtOAc. The combined organic solution was evaporated in vacuo for afford the desired 3-(5-amino-3-oxo-2,3-dihydro-indazol-1-yl)-propionitrile (0.45 g) which was taken into the next reaction without further purification. MS (ESI+): 203.4 ([M+H]+).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationAfter this time the reaction mixture was filtered through Celite® which
  2. washwas washed with more EtOAc
  3. customThe combined organic solution was evaporated in vacuo

출처 및 근거

ORD 기록
ord-6ac2e4b2ede44b8a8780e4893c103deb
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07528158B2

반응 노트

불러오는 중…