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

Propanal → 4-Ethyl-7-trifluoromethyl-4,5-dihydropyrrolo[1,2-a]quinoxaline

HRID 229381
노트
인쇄 미리보기

반응식

HRID 229381 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[C:5]([N+:10]([O-])=O)[CH:4]=1.[CH:15](=O)[CH2:16][CH3:17]>>[CH2:16]([CH:15]1[NH:10][C:5]2[C:6](=[CH:8][CH:9]=[C:3]([C:2]([F:14])([F:13])[F:1])[CH:4]=2)[N:7]2[CH:2]=[CH:3][CH:4]=[C:5]12)[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 527PropanalHCID 67865Benzenamine, 2-nitro-4-(trifluoromethyl)-

생성물 1

HCID 690604574-Ethyl-7-trifluoromethyl-4,5-dihydropyrrolo[1,2-a]quinoxaline

실험 절차

4-Ethyl-7-trifluoromethyl -4,5-dihydropyrrolo[1,2-a]quinoxaline was prepared from 4-trifluoromethyl-2-nitro aniline according to the sequence of Example 1 and 2, and the resulting oil treated with proprionaldehyde according tot he procedure of Example 3 to yield a light orange oil, which was used in the next step without further characterization.

후처리

  1. customto yield a light orange oil, which

출처 및 근거

ORD 기록
ord-8b495574599c48beb37a8c78ec33f9d8
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07563793B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트