反応式
Cl[C:2]1[CH:3]=[C:4]([CH3:20])[C:5]2[NH:6][C:7](=[O:19])[C:8]3[CH:18]=[CH:17][CH:16]=[N:15][C:9]=3[N:10]([CH2:13][CH3:14])[C:11]=2[N:12]=1.[NH2:21][CH2:22][CH2:23][N:24]1[CH2:28][CH2:27][NH:26][C:25]1=[O:29]>>[CH2:13]([N:10]1[C:9]2[N:15]=[CH:16][CH:17]=[CH:18][C:8]=2[C:7](=[O:19])[NH:6][C:5]2[C:4]([CH3:20])=[CH:3][C:2]([NH:21][CH2:22][CH2:23][N:24]3[CH:28]=[CH:27][NH:26][C:25]3=[O:29])=[N:12][C:11]1=2)[CH3:14]参加物
3
実験手順
The title compound, m.p.>300° C., was synthesized from 2-chloro-5,11-dihydro-11-ethyl-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one and 1-(2-aminoethyl)-2-imidazolidone using procedures analogous to those described above, except that the mixture was heated in a pressure bottle at 250° C. for 30 min., and the product was crystallized from acetic acid.
出典と根拠
- ORDレコード
- ord-8f728ddb2d0a4c8fbb4885f5e2e57f70
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05620974
関連ノート
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