2-Chlorobenzothiazole → Benzothiazol-2-yl-(4-chloro-3-methoxy-phenyl)-amine

反応式

Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[Cl:11][C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][C:13]=1[O:19][CH3:20]>>[S:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[NH:16][C:15]1[CH:17]=[CH:18][C:12]([Cl:11])=[C:13]([O:19][CH3:20])[CH:14]=1

参加物

反応物 2

HCID 119872-Chlorobenzothiazole

HCID 131036924-Chloro-3-methoxyaniline

生成物 1

HCID 86017111Benzothiazol-2-yl-(4-chloro-3-methoxy-phenyl)-amine

実験手順

The title compound was synthesised from 2-chloro-benzothiazole (commercially available) and 4-chloro-3-methoxyaniline (commercially available) according to the procedure described for Example 1a) above. MS (m/z): 291.3 (MH+, 100%).

出典と根拠

ORDレコード: ord-1753555d487d471996a0437d232c3d79
出典データセット: uspto-grants-2007_11
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07297707B2

反応ノート

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