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

2-[(2S,3S)-2-methyl-1-[(1S)-1-phenylethyl]pyrrolidin-3-yl]propan-2-ol → (2S,3S)-3-(1-hydroxy-1-methylethyl)-2-methylpyrrolidine

HRID 2046624
노트
인쇄 미리보기

반응식

HRID 2046624 반응식
[CH3:1][C@H:2]1[C@@H:6]([C:7]([OH:10])([CH3:9])[CH3:8])[CH2:5][CH2:4][N:3]1[C@H](C1C=CC=CC=1)C>[C].[Pd].CO>[OH:10][C:7]([C@H:6]1[CH2:5][CH2:4][NH:3][C@H:2]1[CH3:1])([CH3:9])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 686026532-[(2S,3S)-2-methyl-1-[(1S)-1-phenylethyl]pyrrolidin-3-yl]propan-2-ol

생성물 1

HCID 55299039(2S,3S)-3-(1-hydroxy-1-methylethyl)-2-methylpyrrolidine수율 126.9%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

A mixture of 2-[(2S,3S)-2-methyl-1-[(1S)-1-phenylethyl]pyrrolidin-3-yl]propan-2-ol (2.00 g) synthesized by a known method, 10% palladium-carbon (50% water-containing product, 172 mg) and methanol (30 ml) was stirred under a hydrogen atmosphere at room temperature for 60 hr. The catalyst was removed by filtration through celite, and the mother liquor was concentrated. The obtained oily substance was dissolved in methanol, oxalic acid dihydrate (510 mg) was added thereto, and the mixture was concentrated. The residue was crystallized from diethyl ether to give the title compound (1.47 g, 1/2 hydrate).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe catalyst was removed by filtration through celite
  2. concentrationthe mother liquor was concentrated
  3. dissolutionThe obtained oily substance was dissolved in methanol
  4. additionoxalic acid dihydrate (510 mg) was added
  5. concentrationthe mixture was concentrated
  6. customThe residue was crystallized from diethyl ether

출처 및 근거

ORD 기록
ord-e15b48fc1c994864b61acacf11799f91
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592452B2

반응 노트

불러오는 중…