Phosphorus sulfide (P2S5) → 5-(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)thiazole-2-carboxylic acid methyl ester

HRID 644057ノート

反応式

HRID 644057 の反応式
[CH3:1][O:2][C:3](=[O:28])[C:4]([NH:6][CH2:7][C:8]([C:10]1[C:18]2[C:13](=[C:14]([O:19][CH3:20])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH2:21][CH:22]2[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]2)[CH:11]=1)=O)=O.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:30]>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]([C:4]1[S:30][C:8]([C:10]2[C:18]3[C:13](=[C:14]([O:19][CH3:20])[CH:15]=[CH:16][CH:17]=3)[N:12]([CH2:21][CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)[CH:11]=2)=[CH:7][N:6]=1)=[O:28]

参加物

4

実験手順

To a solution of N-[(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)-2-oxo-ethyl]-oxalamic acid methyl ester (429 mg, 1.11 mmol) in chloroform (20 ml) was added phosphorus pentasulfide (538 mg, 1.21 mmol) and the reaction mixture heated at reflux for 3.5 h. The reaction mixture was cooled, poured into a separating funnel and washed with water and then brine. The organic layers were then dried over magnesium sulfate, filtered and the solvent removed in vacuo. The resulting solid was purified by flash column chromatography eluting with dichloromethane to give 5-(1-cyclohexylmethyl-7-methoxy-1H-indol-3-yl)thiazole-2-carboxylic acid methyl ester (418 mg, 1.09 mmol) as a brown solid.

後処理

  1. temperaturethe reaction mixture heated
  2. temperatureat reflux for 3.5 h
  3. temperatureThe reaction mixture was cooled
  4. additionpoured into a separating funnel
  5. washwashed with water
  6. dry with materialThe organic layers were then dried over magnesium sulfate
  7. filtrationfiltered
  8. customthe solvent removed in vacuo
  9. customThe resulting solid was purified by flash column chromatography
  10. washeluting with dichloromethane

出典と根拠

ORDレコード
ord-8bd9412e0c304c57909011c5fbbb5892
出典データセット
uspto-grants-2010_04
特許番号
US07700634B2

反応ノート

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