HCID 22668561, compound → HCID 178460165, compound

HRID 1007414Notes

Reaction equation

HRID 1007414 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.[C:28]([N:32]([CH2:40][CH2:41][CH2:42][N:43]([CH3:45])[CH3:44])[C:33]1[CH:38]=[CH:37][C:36]([NH2:39])=[CH:35][CH:34]=1)(=[O:31])[CH2:29][CH3:30]>>[C:28]([N:32]([C:33]1[CH:38]=[CH:37][C:36]([NH:39]/[C:17](=[C:6]2\[C:5](=[O:27])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=3)/[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:35][CH:34]=1)[CH2:40][CH2:41][CH2:42][N:43]([CH3:44])[CH3:45])(=[O:31])[CH2:29][CH3:30]

Participants

3

Reactant 2

HCID 22668561HCID 22668561, compoundHCID 695643221-Acetyl-3-(1-ethoxy-1-phenylmethylidene)-5,6-dimethoxy-2-indolinone

Product 1

HCID 178460165HCID 178460165, compound

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5,6-dimethoxy-2-indolinone and N-propionyl-N-(3-dimethylamino-propyl)-p-phenylenediamine

Sources & evidence

ORD record
ord-e7f47f2940534ba8bc34731d3bb077d4
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

Loading…