5-Chloro-2-phenoxyaniline → (5-Chloro-2-phenoxy-phenyl)-[1,6]naphthyridin-5-yl-amine

HRID 2358831

反応式

HRID 2358831 の反応式
Cl[C:2]1[N:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.[Cl:12][C:13]1[CH:14]=[CH:15][C:16]([O:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[C:17]([NH2:19])[CH:18]=1>>[Cl:12][C:13]1[CH:14]=[CH:15][C:16]([O:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[C:17]([NH:19][C:2]2[N:11]=[CH:10][CH:9]=[C:8]3[C:3]=2[CH:4]=[CH:5][CH:6]=[N:7]3)[CH:18]=1

参加物

3

反応物 2

HCID 667385-Chloro-2-phenoxyanilineHCID 122042345-Chloro-1,6-naphthyridine

生成物 1

HCID 67249138(5-Chloro-2-phenoxy-phenyl)-[1,6]naphthyridin-5-yl-amine

実験手順

The product from Example 228e (0.040 g, 0.24 mmol) was reacted with the product from Example 42b (0.048 g, 0.24 mmol) for 48 h at 100° C. following the procedure from Example 1g giving the crude title compound which was purified by HPLC with TFA providing the product as a trifluoroacetic acid salt (0.046 g, 40%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 6.96 (d, J=7.35 Hz, 2H) 7.00-7.10 (m, 2 H) 7.22-7.39 (m, 4 H) 7.66 (dd, J=8.46, 4.41 Hz, 1 H) 7.91 (d, J=1.84 Hz, 1 H) 8.07 (d, J=6.25 Hz, 1 H) 8.76 (d, J=8.46 Hz, 1 H) 9.07 (d, J=3.31 Hz, 1 H); MS (ESI+) m/z 348.0 (M+H)+; (ESI−) m/z 346.1 (M−H)−.

出典と根拠

ORDレコード
ord-d504cb4bba0346f68cb89a366c729dc0
出典データセット
uspto-grants-2010_07
特許番号
US07763731B2

関連ノート

読み込み中…