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

(2S)-1,1,1-trifluoropropan-2-yl [(3S)-1-benzylpyrrolidin-3-yl]carbamate → (2S)-1,1,1-trifluoropropan-2-yl (3S)-pyrrolidin-3-ylcarbamate

HRID 452858
노트
인쇄 미리보기

반응식

HRID 452858 반응식
C([N:8]1[CH2:12][CH2:11][C@H:10]([NH:13][C:14](=[O:22])[O:15][C@@H:16]([CH3:21])[C:17]([F:20])([F:19])[F:18])[CH2:9]1)C1C=CC=CC=1>C1COCC1.CO.[OH-].[OH-].[Pd+2]>[NH:8]1[CH2:12][CH2:11][C@H:10]([NH:13][C:14](=[O:22])[O:15][C@@H:16]([CH3:21])[C:17]([F:20])([F:18])[F:19])[CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 68029098(2S)-1,1,1-trifluoropropan-2-yl [(3S)-1-benzylpyrrolidin-3-yl]carbamate

생성물 1

HCID 66697914(2S)-1,1,1-trifluoropropan-2-yl (3S)-pyrrolidin-3-ylcarbamate

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of (2S)-1,1,1-trifluoropropan-2-yl [(3S)-1-benzylpyrrolidin-3-yl]carbamate (1.82 g) in THF (20 ml) and MeOH (20 ml) was added 20% palladium hydroxide on activated carbon (200 mg). The resulting solution was placed under a H2 atmosphere (balloon pressure) and stirred at room temperature for 15 hours. The solution was obtained by filtration through Celite and, washing the filter cake with MeOH, was concentrated in vacuo to give (2S)-1,1,1-trifluoropropan-2-yl(3S)-pyrrolidin-3-ylcarbamate as a pale yellow oil.

후처리

  1. customThe solution was obtained by filtration through Celite
  2. washwashing the filter cake with MeOH
  3. concentrationwas concentrated in vacuo

출처 및 근거

ORD 기록
ord-6780355a699848f7a6255a2ab25e3e63
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492397B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트