3-(1-Ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone → HCID 178464447, compound

HRID 24844Notes

Reaction equation

HRID 24844 reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=2)[NH:13][C:12]1=[O:23])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[OH:24][CH2:25][CH2:26][N:27]([CH2:30][CH2:31][C:32]1[CH:37]=[CH:36][C:35]([NH:38]NC2C=CC=CC=2)=[CH:34][CH:33]=1)[CH2:28][CH3:29]>CN(C=O)C>[OH:24][CH2:25][CH2:26][N:27]([CH2:30][CH2:31][C:32]1[CH:33]=[CH:34][C:35]([NH:38]/[C:4](=[C:11]2\[C:12](=[O:23])[NH:13][C:14]3[C:19]\2=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=3)/[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)=[CH:36][CH:37]=1)[CH2:28][CH3:29]

Participants

4

Procedure

Prepared analogously to Example 89 from 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and {4-[2-(N-(2-hydroxyethyl)-N-ethyl-amino)-ethyl]-phenylamino}-aniline in DMF.

Sources & evidence

ORD record
ord-0f0b8435f743458fa347bb13a77efb83
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

Loading…