Benzenesulfonyl chloride → HCID 178517337, compound

HRID 1007461Notes

Reaction equation

[NH2:1][C:2]1[CH:10]=[C:9]2[C:5](/[C:6](=[C:12](/[NH:19][C:20]3[CH:25]=[CH:24][C:23]([CH2:26][N:27]4[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]4)=[CH:22][CH:21]=3)\[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)/[C:7](=[O:11])[NH:8]2)=[CH:4][CH:3]=1.[C:33]1([S:39](Cl)(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>>[C:33]1([S:39]([NH:1][C:2]2[CH:10]=[C:9]3[C:5](/[C:6](=[C:12](/[NH:19][C:20]4[CH:25]=[CH:24][C:23]([CH2:26][N:27]5[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]5)=[CH:22][CH:21]=4)\[C:13]4[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=4)/[C:7](=[O:11])[NH:8]3)=[CH:4][CH:3]=2)(=[O:41])=[O:40])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1

Participants

Reactant 2

HCID 7369Benzenesulfonyl chloride

HCID 178507260HCID 178507260, compound

Product 1

HCID 178517337HCID 178517337, compound

Procedure

Prepared from 6-amino-3-(Z)-{1-[4-(piperidin-1-yl-methyl)-anilino]-1-phenyl-methylidene}-2-indolinone and benzenesulphonyl chloride

Sources & evidence

ORD record: ord-3ee2cafa5d014348abd483c771d39904
Source dataset: uspto-grants-2004_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06794395B1

Reaction notes

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