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Cesium carbonate → ethyl-(R)-4-(1-carbamoylpropylamino)butyrate

HRID 2197662
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HRID 2197662 반응식
C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:7]([O:9][C:10](=[O:15])[CH2:11][CH2:12][CH2:13][NH2:14])[CH3:8].[C:16]([C@H:19](OS(C)(=O)=O)[CH2:20][CH3:21])(=[O:18])[NH2:17]>C(#N)C>[CH2:7]([O:9][C:10](=[O:15])[CH2:11][CH2:12][CH2:13][NH:14][C@@H:19]([C:16](=[O:18])[NH2:17])[CH2:20][CH3:21])[CH3:8]
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참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 23365gamma-Aminobutyric acid ethyl esterHCID 86617530methanesulfonic acid (R)-1-carbamoyl-propyl ester

생성물 1

HCID 54059837ethyl-(R)-4-(1-carbamoylpropylamino)butyrate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
60 °C

실험 절차

A mixture of powdered caesium carbonate (9.0 g, 27.4 mmol, 5 equiv.), ethyl-4-aminobutyrate (IVb) (1.85 g, 11.0 mmol, 2 equiv.) and methanesulfonic acid (R)-1-carbamoyl-propyl ester (IIi) (1.0 g, 5.5 mmol, 1 equiv.) in acetonitrile (20 ml, 20 vol.) is heated to 60° C. for 16 hours. The mixture is then filtered and the cake rinsed with acetonitrile (50 ml). Combined filtrates are concentrated to dryness under reducd pressure. The crude methyl-(R)-4-(1-carbamoylpropylamino)butyrate is used directly in the next step.

후처리

  1. filtrationThe mixture is then filtered
  2. washthe cake rinsed with acetonitrile (50 ml)
  3. concentrationCombined filtrates are concentrated to dryness under reducd pressure

출처 및 근거

ORD 기록
ord-d6dace805175480cba2f21e509d3e6ba
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338621B2

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