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

HRID 863682
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HRID 863682 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

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

생성물 1

HCID 19696125HCID 19696125, 화합물수율 13.3%

시약·촉매·용매 3

HCID 935Nickel촉매2회HCID 702Ethanol용매HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-9aa3e2ff649d48418bee6db9abced18f
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05721245

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