Water → 9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid methyl ester

HRID 1925561ノート

反応式

HRID 1925561 の反応式
B(Br)(Br)Br.CO[C:7](=[O:23])[C:8]1[CH:17]=[CH:16][CH:15]=[C:10]([C:11]([O:13][CH3:14])=[O:12])[C:9]=1[N:18]1[CH:22]=[CH:21][CH:20]=[CH:19]1.O>ClCCl>[CH3:14][O:13][C:11]([C:10]1[CH:15]=[CH:16][CH:17]=[C:8]2[C:9]=1[N:18]1[CH:19]=[CH:20][CH:21]=[C:22]1[C:7]2=[O:23])=[O:12]

参加物

5

実験手順

In a 50 ml round-bottomed flask, 3 ml of a 1M solution of boron tribromide in dichloromethane are added, at ambient temperature, to a mixture of 260 mg of 2-pyrrol-1-ylisophthalic acid dimethyl ester (which can be prepared according to Helvetica Chim. Acta 1983, 66(7), 2135) dissolved in 4 ml of dichloromethane. The reaction medium is stirred at ambient temperature for 2 hours and then 5 ml of water are added. After separation by settling out, the aqueous phase is re-extracted with twice 15 ml of dichloromethane. The combined organic phases are washed with twice 20 ml of water, dried over magnesium sulphate, and evaporated to dryness under vacuum. The residue is chromatographed on silica gel (15-40 μm), elution being carried out with a mixture of dichloromethane and cyclohexane (50/50 v/v). 122 mg of 9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid methyl ester are obtained in the form of a yellowish solid, the characteristics of which are identical to those of the product obtained by method 1.

後処理

  1. customAfter separation
  2. extractionthe aqueous phase is re-extracted with twice 15 ml of dichloromethane
  3. washThe combined organic phases are washed with twice 20 ml of water
  4. dry with materialdried over magnesium sulphate
  5. customevaporated to dryness under vacuum
  6. customThe residue is chromatographed on silica gel (15-40 μm), elution
  7. additionbeing carried out with a mixture of dichloromethane and cyclohexane (50/50 v/v)

出典と根拠

ORDレコード
ord-1f071fe7d74c42359df1c4c7e35e5759
出典データセット
uspto-grants-2012_05
特許番号
US08178687B2

反応ノート

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