Ethanol → (4-Aminophenyl)(2-methylindolizin-3-yl)methanone
반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[N:9]([C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=1)=[O:12])[CH:8]=[CH:7][CH:6]=[CH:5]2.O.C(O)C>[Zn].C(O)(=O)C>[NH2:19][C:16]1[CH:15]=[CH:14][C:13]([C:11]([C:10]2[N:9]3[C:4]([CH:5]=[CH:6][CH:7]=[CH:8]3)=[CH:3][C:2]=2[CH3:1])=[O:12])=[CH:18][CH:17]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
5.66 g (86.57 mmol) of zinc and 20.63 ml (360.71 mmol) of glacial acetic acid are added to 6.74 g (24.05 mmol) of (2-methylindolizin-3-yl)(4-nitrophenyl)methanone in 120 ml of a 2/1 mixture of water and ethanol. The reaction medium is heated at 80° C. for 4 hours. 0.57 g (8.7 mmol) of zinc and 2.06 ml of glacial acetic acid are added. Refluxing is maintained for 1 hour. At ambient temperature, the reaction medium is filtered off. The residue obtained is rinsed with ethyl acetate and with methyl THF. The organic phase is washed with a saturated aqueous solution of sodium hydrogen carbonate and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate, and then concentrated under reduced pressure. The residue obtained is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (90/10) mixture. 4.9 g of a yellow solid are obtained.
후처리
- temperatureRefluxing
- temperatureis maintained for 1 hour
- filtrationAt ambient temperature, the reaction medium is filtered off
- customThe residue obtained
- washis rinsed with ethyl acetate and with methyl THF
- washThe organic phase is washed with a saturated aqueous solution of sodium hydrogen carbonate
- dry with materialwith a saturated aqueous solution of sodium chloride, dried over sodium sulphate
- concentrationconcentrated under reduced pressure
- customThe residue obtained
- customis purified by silica gel column chromatography, elution
출처 및 근거
- ORD 기록
- ord-1e2c03663d6d4639874783a094d84a6a
- 출처 데이터셋
- uspto-grants-2014_10
- 특허 번호
- US08859544B2
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