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Dimethylformamide → 1-(3-Benzyloxy-phenyl)-8-chloro-3-methylsulfanyl-imidazo[1,5-a]pyrazine

HRID 1992427
ノート
印刷プレビュー

反応式

HRID 1992427 の反応式
[CH3:1][S:2][C:3](=O)[NH:4][CH:5]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:14]=1)[C:6]1[C:11]([Cl:12])=[N:10][CH:9]=[CH:8][N:7]=1.CN(C=O)C.O=P(Cl)(Cl)Cl>CC#N>[CH2:20]([O:19][C:15]1[CH:14]=[C:13]([C:5]2[N:4]=[C:3]([S:2][CH3:1])[N:7]3[CH:8]=[CH:9][N:10]=[C:11]([Cl:12])[C:6]=23)[CH:18]=[CH:17][CH:16]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 58902032[(3-benzyloxy-phenyl)-(3-chloro-pyrazin-2-yl)-methyl]-thiocarbamic acid S-methyl ester

生成物 1

HCID 589020221-(3-Benzyloxy-phenyl)-8-chloro-3-methylsulfanyl-imidazo[1,5-a]pyrazine

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
55 °C

実験手順

To a solution of [(3-benzyloxy-phenyl)-(3-chloro-pyrazin-2-yl)-methyl]-thiocarbamic acid S-methyl ester (200 mg, 0.0005 mol) in MeCN (10 mL) and DMF (0.12 mL, 0.0015 mol) was added POCl3 (0.14 mL, 0.0015 mol); the resulting mixture was stirred at 55° C. overnight. The mixture was quenched with 2N NH3/iPrOH, then diluted with EtOAc, washed with brine and dried over anhydrous sodium sulfate. The residue was purified by silica gel chromatography (Hex.: EtOAc=80:20→70:30) to give a yellow solid. 1H-NMR (CDCl3) confirmed a mixture of the desired product and starting material in ca. 1:1 ratio, which was taken on to next step.

後処理

  1. customThe mixture was quenched with 2N NH3/iPrOH
  2. additiondiluted with EtOAc
  3. washwashed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe residue was purified by silica gel chromatography (Hex.: EtOAc=80:20→70:30)
  6. customto give a yellow solid

出典と根拠

ORDレコード
ord-13c2a1593384416fbea174c5602fa00d
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07648987B2

反応ノート

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