4-(Piperidin-1-ylmethyl)aniline → HCID 178517188, compound

HRID 1007441Notes

Reaction equation

HRID 1007441 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([F:16])([F:15])[F:14])[CH:11]=2)[C:6](=[C:17](Cl)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:5]1=[O:25])(=O)C.[N:26]1([CH2:32][C:33]2[CH:39]=[CH:38][C:36]([NH2:37])=[CH:35][CH:34]=2)[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1>>[N:26]1([CH2:32][C:33]2[CH:34]=[CH:35][C:36]([NH:37]/[C:17](=[C:6]3\[C:5](=[O:25])[NH:4][C:12]4[C:7]\3=[CH:8][CH:9]=[C:10]([C:13]([F:15])([F:14])[F:16])[CH:11]=4)/[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:38][CH:39]=2)[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]1

Participants

3

Procedure

Prepared from 1-acetyl-3-(1-chloro-1-phenyl-methylidene)-6-trifluoromethyl-2-indolinone and 4-(piperidin-1-yl-methyl)-aniline

Sources & evidence

ORD record
ord-967c08ba3e9a44718ad3bc64d260fdc8
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

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