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Dimethylformamide → Tert-butyl (1-(3-chloropyrazin-2-yl)pyrrolidin-3-yl)carbamate

HRID 907561
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인쇄 미리보기

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HRID 907561 반응식
Cl[C:2]1[C:7]([Cl:8])=[N:6][CH:5]=[CH:4][N:3]=1.C(C1CCN(N)C1)([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=O.C[N:23]([CH:25]=[O:26])[CH3:24]>>[C:12]([O:11][C:25](=[O:26])[NH:23][CH:24]1[CH2:7][CH2:2][N:3]([C:2]2[C:7]([Cl:8])=[N:6][CH:5]=[CH:4][N:3]=2)[CH2:4]1)([CH3:15])([CH3:14])[CH3:13]
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참가 물질

4

반응물 3

HCID 6228Dimethylformamide2회HCID 785752,3-DichloropyrazineHCID 21876723Tert-butyl 1-aminopyrrolidine-3-carboxylate

생성물 1

HCID 59013776Tert-butyl (1-(3-chloropyrazin-2-yl)pyrrolidin-3-yl)carbamate

반응 조건

온도
100 °C

실험 절차

To a round bottom flask equipped with a magnetic stir bar was added 2,3-Dichloro-pyrazine (3 g, 20.2 mmol) and dry DMF (50 mL). 3-Boc-aminopyrrolidine (8.2 g, 44.5 mmol) was dissolved in dry DMF (50 mL) and added to the round bottom flask. The reaction mixture was allowed to continue to stir overnight at 100° C. LC/MS analysis indicated the desired product as the main component. The reaction mixture was cooled to room temperature and poured on ice. The mixture was extracted with EtOAc and the EtOAc layer was washed with water and brine and dried on sodium sulfate. After removal of solvent in vacuo the desired product [1-(3-Chloro-pyrazin-2-yl)-pyrrolidin-3-yl]-carbamic acid tert-butyl ester (6.8 g, 99% yield) was obtained.

후처리

  1. customTo a round bottom flask equipped with a magnetic stir bar
  2. additionadded to the round bottom flask

출처 및 근거

ORD 기록
ord-0a3e25ed7ef7495a818e15f086d4f264
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08013156B2

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