4-(Piperidin-1-ylmethyl)aniline → HCID 178487306, compound

Reaction equation

C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:15](OCC)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=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:15](=[C:6]3\[C:5](=[O:25])[NH:4][C:12]4[C:7]\3=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=4)/[C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:38][CH:39]=2)[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]1

Participants

Reactant 2

HCID 8461504-(Piperidin-1-ylmethyl)aniline

HCID 695646841-Acetyl-3-(1-ethoxy-1-phenyl-methylidene)-6-methoxy-2-indolinone

Product 1

HCID 178487306HCID 178487306, compound

Procedure

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

Sources & evidence

ORD record: ord-e6019beecd50443ebf31379a5307ee9d
Source dataset: uspto-grants-2004_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06794395B1

Reaction notes

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