(4-Aminophenyl)(piperidin-1-yl)methanone → HCID 178486542, compound

HRID 1007416Notes

Reaction equation

HRID 1007416 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:17](OCC)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:5]1=[O:27])(=O)C.[N:28]1([C:34]([C:36]2[CH:42]=[CH:41][C:39]([NH2:40])=[CH:38][CH:37]=2)=[O:35])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1>>[N:28]1([C:34]([C:36]2[CH:37]=[CH:38][C:39]([NH:40]/[C:17](=[C:6]3\[C:5](=[O:27])[NH:4][C:12]4[C:7]\3=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=4)/[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:41][CH:42]=2)=[O:35])[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1

Participants

3

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5,6-dimethoxy-2-indolinone and 4-(piperidin-1-yl-carbonyl)-aniline

Sources & evidence

ORD record
ord-cea7b31390134a45a5410dafcef12c99
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

Loading…