Tert-butyl 2-(4-aminophenyl)acetate → HCID 178468587, compound

HRID 1883824Notes

Reaction equation

HRID 1883824 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=2)[C:6](=[C:18](OCC)[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:5]1=[O:28])(=O)C.[NH2:29][C:30]1[CH:35]=[CH:34][C:33]([CH2:36][C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])=[CH:32][CH:31]=1>>[C:40]([O:39][C:37]([CH2:36][C:33]1[CH:34]=[CH:35][C:30]([NH:29]/[C:18](=[C:6]2\[C:5](=[O:28])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=3)/[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:31][CH:32]=1)=[O:38])([CH3:43])([CH3:41])[CH3:42]

Participants

3

Reactant 2

HCID 2760930Tert-butyl 2-(4-aminophenyl)acetateHCID 685275611-Acetyl-3-(1-ethoxy-1-phenylmethylene)-6-ethoxycarbonyl-2-indolinone

Product 1

HCID 178468587HCID 178468587, compound

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-ethoxycarbonyl-2-indolinone and tert.butyl 4-aminophenylacetate Rf value: 0.5 (aluminium oxide, ethyl acetate) C30H30N2O5

Sources & evidence

ORD record
ord-67fd84cb6aa04f54bd4aefef87450134
Source dataset
uspto-grants-2004_07
Patent number
US06762180B1

Reaction notes

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