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Dicyclohexylcarbodiimide → N-(2-Amino-2-oxoethyl)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide

HRID 621604
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HRID 621604 반응식
[OH:1][CH:2]1[CH2:6][N:5]([CH2:7][C:8]([OH:10])=O)[C:4](=[O:11])[CH2:3]1.[NH2:12][CH2:13][C:14]([NH2:16])=[O:15].C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[OH:1][CH:2]1[CH2:6][N:5]([CH2:7][C:8]([NH:12][CH2:13][C:14]([NH2:16])=[O:15])=[O:10])[C:4](=[O:11])[CH2:3]1
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참가 물질

5

반응물 3

HCID 10868DicyclohexylcarbodiimideHCID 69020GlycinamideHCID 111265411-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (+-)-

생성물 1

HCID 11701304N-(2-Amino-2-oxoethyl)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide수율 51.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To an ice-cold mixture of 4-hydroxy-2-oxo-1-pyrrolidineacetic acid (1 g) and glycinamide (700 mg) in dimethylformamide (20 ml), dicyclohexylcarbodiimide (1.3 g) was added at once. Stirring was continued for 5 hours at room temperature, then the solvent was removed under vacuum. The residue was suspended in water (20 ml) and stirred for 30 minutes at room temperature. The insoluble material was filtered off and the filtrate evaporated to dryness. The residue was triturated with 2-propanol to yield the title compound (700 mg).

후처리

  1. additionwas added at once
  2. customthe solvent was removed under vacuum
  3. stirringstirred for 30 minutes at room temperature
  4. filtrationThe insoluble material was filtered off
  5. customthe filtrate evaporated to dryness
  6. customThe residue was triturated with 2-propanol

출처 및 근거

ORD 기록
ord-645738f1cb21459892ec26809a9f7061
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824861

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