반응식
[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][C:9]([F:15])=[C:10](F)[C:11]=2[F:13])[C:6](=[O:16])[C:5]([C:17]([OH:19])=[O:18])=[CH:4]1)[CH3:2].[NH2:20][CH2:21][CH:22]1[CH:26]([CH3:27])[CH2:25][NH:24][CH2:23]1.C1CCN2C(=NCCC2)CC1>C(#N)C>[NH2:20][CH2:21][CH:22]1[CH:26]([CH3:27])[CH2:25][N:24]([C:10]2[C:11]([F:13])=[C:12]3[C:7]([C:6](=[O:16])[C:5]([C:17]([OH:19])=[O:18])=[CH:4][N:3]3[CH2:1][CH3:2])=[CH:8][C:9]=2[F:15])[CH2:23]1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (0.5 g), anhydrous acetonitrile (5 ml), 3-aminomethyl-4-methylpyrrolidine (0.22 g) and DBU (0.28 g) was refluxed for an hour and then stirred at room temperature for 3 hours. The resulting precipitate was collected by filtration and washed with ether to give the title compound (0.39 g) as pale yellow powder, mp 222°-224° C.
후처리
- temperaturewas refluxed for an hour
- filtrationThe resulting precipitate was collected by filtration
- washwashed with ether
출처 및 근거
- ORD 기록
- ord-4f53e47eedaa4744a3b0dfd901419858
- 출처 데이터셋
- uspto-grants-1988_06
- 특허 번호
- US04753953
연결된 노트
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