HCID 16782538, compound → HCID 178517270, compound

HRID 24870Notes

Reaction equation

HRID 24870 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][CH:25]1[CH2:30][CH2:29][N:28]([CH2:31][C:32]2[CH:38]=[CH:37][C:35]([NH2:36])=[CH:34][CH:33]=2)[CH2:27][CH2:26]1>CN(C=O)C>[OH:24][CH:25]1[CH2:26][CH2:27][N:28]([CH2:31][C:32]2[CH:38]=[CH:37][C:35]([NH:36]/[C:4](=[C:11]3\[C:12](=[O:23])[NH:13][C:14]4[C:19]\3=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=4)/[C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=3)=[CH:34][CH:33]=2)[CH2:29][CH2:30]1

Participants

4

Reactant 2

HCID 16782538HCID 16782538, compoundHCID 537348873-(1-Ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone

Product 1

HCID 178517270HCID 178517270, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Prepared analogously to Example 89 from 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-(4-hydroxypiperidinomethyl)-aniline in DMF.

Sources & evidence

ORD record
ord-e03de1f518eb40f793686019f5c59614
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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