3,4-Difluorobenzylamine → HCID 59474765、化合物

反応式

Cl[C:2]1[C:11]2[C:6](=[C:7]([S:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1.[F:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][C:23]=1[F:24])[CH2:19][NH2:20]>>[F:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][C:23]=1[F:24])[CH2:19][NH:20][C:2]1[C:11]2[C:6](=[C:7]([S:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1

参加物

反応物 2

HCID 1235723,4-Difluorobenzylamine

HCID 2331984-Chloro-2-methyl-8-methylsulfanylquinoline

生成物 1

HCID 59474765HCID 59474765、化合物

実験手順

Preparation was made using a similar procedure as described in example 1, method 1.3. Starting materials were 4-chloro-2-methyl-8-methylsulfanylquinoline and 3,4-difluorobenzylamine.

後処理

customPreparation

出典と根拠

ORDレコード: ord-460f049ed71b45bfa7d954d257a01336
出典データセット: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08420670B2

反応ノート

読み込み中…