2-Chloro-5-methylaniline → 3-N-(2-chloro-5-methylphenyl)-4-methoxyisophthalamide

HRID 646328

反応式

HRID 646328 の反応式
[CH3:1][O:2][C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([C:12]([NH2:14])=[O:13])=[CH:5][CH:4]=1.[Cl:15][C:16]1[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][C:17]=1[NH2:18]>>[Cl:15][C:16]1[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][C:17]=1[NH:18][C:9](=[O:11])[C:8]1[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=1[O:2][CH3:1])[C:12]([NH2:14])=[O:13]

参加物

3

反応物 2

HCID 667702-Chloro-5-methylanilineHCID 132228085-Carbamoyl-2-methoxybenzoic acid

生成物 1

HCID 592650663-N-(2-chloro-5-methylphenyl)-4-methoxyisophthalamide

実験手順

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 2-chloro-5-methylaniline by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

出典と根拠

ORDレコード
ord-4eb72c2136b3449abab6af2a7d7686fc
出典データセット
uspto-grants-2010_04
特許番号
US07705053B2

関連ノート

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