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Ethyl 1-oxo-2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylate → HCID 19696125、化合物

HRID 863682
ノート
印刷プレビュー

反応式

HRID 863682 の反応式
O=[C:2]1[C:6]2=[CH:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[N:5]2[CH2:4][CH:3]1[C:14]([O:16][CH2:17][CH3:18])=[O:15]>[Ni].C(O)C.O>[CH2:2]1[C:6]2=[CH:7][C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[N:5]2[CH2:4][CH:3]1[C:14]([O:16][CH2:17][CH3:18])=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 12582025Ethyl 1-oxo-2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylate

生成物 1

HCID 19696125HCID 19696125、化合物収率 13.3%

試薬・触媒・溶媒 3

HCID 935Nickel触媒2 回HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

6 spoon spatula measures of Raney nickel were added to a solution of 5.08 g of ethyl 2,3-dihydro-1-oxo-1H-pyrrolo[1,2-a]indole-2-carboxylate in 180 ml of ethanol and 90 ml of water. The mixture was heated to reflux for 10 hours. Then, an additional 3 spoon spatula measures of Raney nickel were added. Heating was continued for 5.5 hours, whereupon the mixture was cooled and filtered. The filter residue was washed with ethyl acetate and dichloromethane. The combined filtrate and washings were evaporated and the residue was purified by chromatography on silica gel with diethyl ether/petroleum ether (1:2). Crystallization from methanol gave 635 mg of ethyl 2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylate of melting point 55°-57° C.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 10 hours
  3. temperatureHeating
  4. temperaturewas cooled
  5. filtrationfiltered
  6. washThe filter residue was washed with ethyl acetate and dichloromethane
  7. customThe combined filtrate and washings were evaporated
  8. customthe residue was purified by chromatography on silica gel with diethyl ether/petroleum ether (1:2)
  9. customCrystallization from methanol

出典と根拠

ORDレコード
ord-9aa3e2ff649d48418bee6db9abced18f
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05721245

反応ノート

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