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Phosphorus oxychloride → 3-(2-Chloroethyl)imidazo[1,5-a]pyrazine

HRID 566250
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HRID 566250 반응식
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[CH2:7][NH:8][C:9](=O)[CH2:10][CH2:11][Cl:12].P(Cl)(Cl)(Cl)=O>ClCCl>[Cl:12][CH2:11][CH2:10][C:9]1[N:1]2[CH:6]=[CH:5][N:4]=[CH:3][C:2]2=[CH:7][N:8]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 21265851N-(2-pyrazinylmethyl)-3-chloropropionamide

생성물 1

HCID 212658743-(2-Chloroethyl)imidazo[1,5-a]pyrazine수율 74.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of N-(2-pyrazinylmethyl)-3-chloropropionamide (4.52 g) in dichloromethane (30 ml) was added phosphorus oxychloride (1.29 g) under ice cooling. The mixture was stirred for 3 days at room temperature. The mixture was concentrated, and the residue was poured into ice water (400 ml), followed by neutralization with sodium carbonate. The reaction mixture was subjected to salting out with sodium chloride, and extracted with ethyl acetate-THF (1:1, 150 ml×3). The organic layers were combined and dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was subjected to flash column chromatography [carrier: silica gel, 100 g, developing solvent: ethyl acetate→ethyl acetate-ethanol (9:1)]. The eluate was concentrated and residual solid was washed with diethylether to give the title compound (3.07 g) as colorless solid product.

후처리

  1. concentrationThe mixture was concentrated
  2. additionthe residue was poured into ice water (400 ml)
  3. extractionextracted with ethyl acetate-THF (1:1, 150 ml×3)
  4. dry with materialdried over magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. concentrationThe eluate was concentrated
  7. washresidual solid was washed with diethylether

출처 및 근거

ORD 기록
ord-b88d7951211d4d7f9dcd0c0bec763463
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06174877B1

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