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Potassium Carbonate → (S)-1-(3-hydroxypropyl)pyrrolidine-2-carboxamide

HRID 1838584
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HRID 1838584 반응식
Br[CH2:2][CH2:3][CH2:4][OH:5].[NH:6]1[CH2:10][CH2:9][CH2:8][C@H:7]1[C:11]([NH2:13])=[O:12].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[OH:5][CH2:4][CH2:3][CH2:2][N:6]1[CH2:10][CH2:9][CH2:8][C@H:7]1[C:11]([NH2:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 123083-Bromo-1-propanolHCID 111306L-Prolinamide

생성물 1

HCID 45116058(S)-1-(3-hydroxypropyl)pyrrolidine-2-carboxamide수율 60.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3-Bromo-1-propanol (584 mg, 4.2 mmol) was added to a mixture of (S)-pyrrolidine-2-carboxamide (399 mg, 3.5 mmol) and potassium carbonate (966 mg, 7 mmol) in acetonitrile (10 ml). The mixture was heated at reflux for 5 hours and the mixture was stirred for 18 hours at ambient temperature. The insolubles were removed by filtration and the solvent was removed from the filtrate by evaporation. The residue was purified by column chromatography on silica eluting with methylene chloride/methanol (9/1 followed by 8/2) to give (S)-1-(3-hydroxypropyl)-pyrrolidine-2-carboxamide (365 mg, 60%).

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후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 5 hours
  3. customThe insolubles were removed by filtration
  4. customthe solvent was removed from the filtrate by evaporation
  5. customThe residue was purified by column chromatography on silica eluting with methylene chloride/methanol (9/1 followed by 8/2)

출처 및 근거

ORD 기록
ord-63777e87f6734e92a196e158860ed5bf
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06673803B2

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