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

HCID 86679676, 화합물 → HCID 86679678, 화합물

HRID 577751
노트
인쇄 미리보기

반응식

HRID 577751 반응식
C([N:8]1[CH2:12][C@@H:11]([N+:13]([O-])=O)[C@H:10]([CH:16]([F:18])[F:17])[CH2:9]1)C1C=CC=CC=1>CO>[F:17][CH:16]([F:18])[C@@H:10]1[CH2:9][NH:8][CH2:12][C@H:11]1[NH2:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86679676HCID 86679676, 화합물

생성물 1

HCID 86679678HCID 86679678, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of trans-1-benzyl-3-(difluoromethyl)-4-nitropyrrolidine (25 g, 0.097 mol) and Pd (OH)2/C (4 g) in MeOH (200 mL) was placed under a hydrogen atmosphere (50 psi) at rt overnight. The mixture was filtered to yield trans-4-(difluoromethyl)pyrrolidin-3-amine in solution. Boc2O was added at 0° C. and the resulting mixture was stirred at 0° C. for 4 hrs, then concentrated and purified by column chromatography (100% EtOAc) to give the title compound (14 g, 61% yield) as a yellow oil.

후처리

  1. customat rt
  2. customovernight
  3. filtrationThe mixture was filtered

출처 및 근거

ORD 기록
ord-6335b70ee76247609623d3035df3e05d
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040547B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트