2-Butanol, 4-amino- → 4-Chloro-6-{(2-chlorophenyl)[(3-hydroxybutyl)amino]methylidene}cyclohexa-2,4-dien-1-one

反応式

[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1[OH:17])=O.[NH2:18][CH2:19][CH2:20][CH:21]([OH:23])[CH3:22]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[N:18][CH2:19][CH2:20][CH:21]([OH:23])[CH3:22])[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1[OH:17]

参加物

反応物 2

HCID 1702542-Butanol, 4-amino-

HCID 27359952',5-Dichloro-2-hydroxybenzophenone

生成物 1

HCID 1354573554-Chloro-6-{(2-chlorophenyl)[(3-hydroxybutyl)amino]methylidene}cyclohexa-2,4-dien-1-one

実験手順

The enantiomers of this compound were prepared in the same manner by a reaction between (2-chlorophenyl)-(5-chloro-2-hydroxyphenyl)-methanone and the enantiomers of 4-aminobutan-2-ol.

出典と根拠

ORDレコード: ord-6812d6f48c664711a3110368ee0598f4
出典データセット: uspto-grants-1986_01
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04564636

反応ノート

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