Benzamide, N-(4-aminophenyl)- → N-[4-(9-Trifluoromethyl-6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-ylamino)-phenyl]-benzamide

HRID 1029262

反応式

HRID 1029262 の反応式
Cl[C:2]1[CH:11]=[CH:10][N:9]=[C:8]2[C:3]=1[C:4]1[CH:16]=[C:15]([C:17]([F:20])([F:19])[F:18])[CH:14]=[CH:13][C:5]=1[C:6](=[O:12])[NH:7]2.[NH2:21][C:22]1[CH:27]=[CH:26][C:25]([NH:28][C:29](=[O:36])[C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[CH:24][CH:23]=1>>[F:18][C:17]([F:20])([F:19])[C:15]1[CH:14]=[CH:13][C:5]2[C:6](=[O:12])[NH:7][C:8]3[C:3]([C:4]=2[CH:16]=1)=[C:2]([NH:21][C:22]1[CH:27]=[CH:26][C:25]([NH:28][C:29](=[O:36])[C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[CH:24][CH:23]=1)[CH:11]=[CH:10][N:9]=3

参加物

3

反応物 2

HCID 87196Benzamide, N-(4-aminophenyl)-HCID 686488171-chloro-9-trifluoromethyl-5H-benzo[c][1,8]naphthyridin-6-one

生成物 1

HCID 44208006N-[4-(9-Trifluoromethyl-6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-ylamino)-phenyl]-benzamide

実験手順

The title compound was synthesized according to the procedure described for the preparation of Example 378, method 2 using 1-chloro-9-trifluoromethyl-5H-benzo[c][1,8]naphthyridin-6-one and N-(4-amino-phenyl)-benzamide to provide 403. LC-MS (M+H=475, obsd.=475). 1H NMR (400 MHz, DMSO-d6): δ 6.96 (d, 1H), 7.18 (d, 2H), 7.54 (m, 3H), 7.76 (m, 2H), 7.78 (d, 1H), 7.97 (d, 1H), 8.10 (d, 1H), 8.27 (s, 1H), 8.85 (d, 1H), 8.99 (s, 1H), 10.25 (s, 1H).

後処理

  1. customThe title compound was synthesized

出典と根拠

ORDレコード
ord-2e6199cc19dd47cdbc511c14cde2d138
出典データセット
uspto-grants-2014_05
特許番号
US08735584B2

関連ノート

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