Aniline → N-Phenyl-3-(1-piperidinylsulfonyl)benzamide

反応式

[N:1]1([S:7]([C:10]2[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=2)[C:13]([OH:15])=O)(=[O:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[NH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:20]1([NH:19][C:13](=[O:15])[C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([S:7]([N:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)(=[O:8])=[O:9])[CH:11]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

反応物 2

HCID 6115Aniline

HCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

生成物 1

HCID 558837N-Phenyl-3-(1-piperidinylsulfonyl)benzamide

実験手順

The entitled compound was produced according to the method of Example 73 but using 3-(piperidin-1-ylsulfonyl)benzoic acid and aniline as the starting materials.

後処理

customThe entitled compound was produced

出典と根拠

ORDレコード: ord-dc9fcdd427f2482d99f2e0035aa731e8
出典データセット: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08420823B2

反応ノート

読み込み中…