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Methanol → Acetamide, N-methyl-N-[4-(3-hydroxypyrrolidinyl)-2-butynyl]-

HRID 2107985
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인쇄 미리보기

반응식

HRID 2107985 반응식
C([O:4][CH:5]1[CH2:9][CH2:8][N:7]([CH2:10][C:11]#[C:12][CH2:13][N:14]([CH3:18])[C:15](=[O:17])[CH3:16])[CH2:6]1)(=O)C.C(=O)([O-])[O-].[Na+].[Na+].CO>ClCCl>[OH:4][CH:5]1[CH2:9][CH2:8][N:7]([CH2:10][C:11]#[C:12][CH2:13][N:14]([CH3:18])[C:15](=[O:17])[CH3:16])[CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 10340Sodium CarbonateHCID 15086787(Racemic)-N-[4-[3-(Acetyloxy)-1-pyrrolidinyl]-2-butynyl]-N-methyl acetamide

생성물 1

HCID 536669Acetamide, N-methyl-N-[4-(3-hydroxypyrrolidinyl)-2-butynyl]-수율 73.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 820 mg of (racemic)-N-[4-[3-(acetyloxy)-1-pyrrolidinyl]-2-butynyl]-N-methyl acetamide, 635 mg of sodium carbonate and 40 ml of methanol was stirred overnight. An equal volume of dichloromethane was added, the mixture filtered and the solvents concentrated. This residue was purified by chromatography (alumina), giving 500 mg of the desired product as a yellow oil.

후처리

  1. filtrationthe mixture filtered
  2. concentrationthe solvents concentrated
  3. customThis residue was purified by chromatography (alumina)

출처 및 근거

ORD 기록
ord-c7ae12738e334b13a5dd19a0ecc86d49
출처 데이터셋
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04937235

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