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

HRID 566250
ノート
印刷プレビュー

反応式

HRID 566250 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-b88d7951211d4d7f9dcd0c0bec763463
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06174877B1

反応ノート

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