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

Triethylamine → (S)-1-Boc-3-methanesulfonyloxy-pyrrolidine

HRID 873335
노트
인쇄 미리보기

반응식

HRID 873335 반응식
[OH:1][C@H:2]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]1.C(N(CC)CC)C.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>C(Cl)Cl>[CH3:21][S:22]([O:1][C@H:2]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]1)(=[O:24])=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 854055tert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylate

생성물 1

HCID 11032777(S)-1-Boc-3-methanesulfonyloxy-pyrrolidine수율 123.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of (S)-tert-butyl 3-hydroxypyrrolidine-1-carboxylate (200 mg, 1.07 mmol) and triethylamine (0.3 mL, 1.07 mmol) in DCM (10 mL) at 0° C. was added methane sulfonylchloride (0.125 mL, 1.07 mmol) dropwise. After stirring for 3 h, the reaction mixture was washed with sat. NaHCO3 solution (aq.). The aqueous layer was extracted with DCM and the combined organics were dried (MgSO4), filtered and concentrated in vacuo to give the title compound (350 mg) as a colourless solid which was used in the next step without further purification.

후처리

  1. washthe reaction mixture was washed with sat. NaHCO3 solution (aq.)
  2. extractionThe aqueous layer was extracted with DCM
  3. dry with materialthe combined organics were dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-640cadd9b27f4fd687508002612dd179
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08975406B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트