반응식
[Al+3].[Cl-].[Cl-].[Cl-].[Na+].[Cl-].[CH2:7]1[C:17]2=[C:18]3[C:13](=[CH:14][CH:15]=[CH:16]2)[CH2:12][CH2:11][C:10](=[O:19])[N:9]3[CH2:8]1.Cl.[C:21](Cl)(=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[N:24][CH:23]=1.Cl>C(O)C.O>[N:24]1[CH:25]=[CH:26][CH:27]=[C:22]([C:21]([C:15]2[CH:14]=[C:13]3[C:18]4=[C:17]([CH2:7][CH2:8][N:9]4[C:10](=[O:19])[CH2:11][CH2:12]3)[CH:16]=2)=[O:28])[CH:23]=1참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
To a molten mixture of AlCl3 (8.0 g, 60.0 mmol) and NaCl (2.34 g, 40.0 mmol) at 150° C. was added 1,2,5,6-tetrahydro-pyrrolo[3,2,1-ij]quinolin-4-one (1.79 g, 10.0 mmol) and thereafter nicotinoylchloride hydrochloride salt (1.96 g, 11.0 mmol) portionwise. After stirring for 15 min and cooling to room temperature, excess aluminum chloride was decomposed by the addition of a chilled mixture of 10 ml concentrated hydrochloric acid and 200 ml water. Neutralization with NaHCO3 solution and subsequent extraction with ethyl acetate (3×100 ml), followed by drying over MgSO4 and removal of the solvent gave the crude product. Purification by crystallization from ethanol gave the acylation product (624 mg, 2.24 mmol, 22%) as a yellow solid, mp (ethanol) 147° C. 1H-NMR (500 MHz, CDCl3): δ=2.72 (t, 3J=7.9 Hz, 2H), 3.02 (t, 3J=7.9 Hz, 2H), 3.23 (t, 3J=8.6 Hz, 2H), 4.14 (t, 3J=8.6 Hz, 2H), 7.44 (ddd, 3J=7.9 Hz, 3J=4.7 Hz, 5J=1.0 Hz, 1H), 7.53 (s, 1H), 7.58 (s, 1H), 8.06 (m, 1H), 8.78 (dd, 3J=5.0 Hz, 4J=1.9 Hz, 1H), 8.92 (dd, 4J=1.9 Hz, 5J=0.8 Hz, 1H). 13C-NMR (125 MHz, CDCl3): δ=24.2, 27.3, 31.4, 45.8, 199.9, 123.4, 126.1, 128.9, 129.4, 132.3, 134.0, 137.0, 146.1, 150.4, 152.4, 167.8, 193.6. MS m/z 278.79 (MH+).
후처리
- extractionNeutralization with NaHCO3 solution and subsequent extraction with ethyl acetate (3×100 ml)
- dry with materialby drying over MgSO4 and removal of the solvent
- customgave the crude product
- customPurification
- customby crystallization from ethanol
출처 및 근거
- ORD 기록
- ord-65f42044164a4c2e93c4763e6f251c5c
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08541404B2
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