3,4-Dichlorobenzaldehyde → [3-(3-Benzyl-8-chlorocinnolin-4-yl)phenyl](3,4-dichlorobenzyl)amine

反応式

[CH2:1]([C:8]1[N:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:25])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:26][C:27]1[CH:28]=[C:29]([CH:32]=[CH:33][C:34]=1[Cl:35])[CH:30]=O>>[CH2:1]([C:8]1[N:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:30][C:29]3[CH:32]=[CH:33][C:34]([Cl:35])=[C:27]([Cl:26])[CH:28]=3)[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:25])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

反応物 2

HCID 227103,4-Dichlorobenzaldehyde

HCID 11855621[3-(3-Benzyl-8-chlorocinnolin-4-yl)phenyl]amine

生成物 1

HCID 11854830[3-(3-Benzyl-8-chlorocinnolin-4-yl)phenyl](3,4-dichlorobenzyl)amine

実験手順

The title compound was prepared from [3-(3-benzyl-8-chlorocinnolin-4-yl)phenyl]amine and 3,4-dichlorobenzaldehyde according to the procedure of Step 5 Example 6. MS (ES) m/z 504.6.

出典と根拠

ORDレコード: ord-c64fb6d34f404a69aa7244300fb15943
出典データセット: uspto-grants-2010_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07700595B2

反応ノート

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