4-(4-Methoxypiperidinomethyl)-aniline → HCID 178493121, compound

HRID 24873Notes

Reaction equation

HRID 24873 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.[CH3:24][O:25][CH:26]1[CH2:31][CH2:30][N:29]([CH2:32][C:33]2[CH:39]=[CH:38][C:36]([NH2:37])=[CH:35][CH:34]=2)[CH2:28][CH2:27]1>CN(C=O)C>[CH3:24][O:25][CH:26]1[CH2:31][CH2:30][N:29]([CH2:32][C:33]2[CH:34]=[CH:35][C:36]([NH:37]/[C:4](=[C:11]3\[C:12](=[O:23])[NH:13][C:14]4[C:15]\3=[CH:16][C:17]([N+:20]([O-:22])=[O:21])=[CH:18][CH:19]=4)/[C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=3)=[CH:38][CH:39]=2)[CH2:28][CH2:27]1

Participants

4

Reactant 2

HCID 225695044-(4-Methoxypiperidinomethyl)-anilineHCID 537348873-(1-Ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone

Product 1

HCID 178493121HCID 178493121, 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-methoxypiperidinomethyl)-aniline in DMF.

Sources & evidence

ORD record
ord-a4499642ded9493187b9b094375055f9
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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