4-[(Azetidin-1-yl)methyl]aniline → HCID 178517258, compound

HRID 24930Notes

Reaction equation

HRID 24930 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.[N:24]1([CH2:28][C:29]2[CH:35]=[CH:34][C:32]([NH2:33])=[CH:31][CH:30]=2)[CH2:27][CH2:26][CH2:25]1>>[N:24]1([CH2:28][C:29]2[CH:35]=[CH:34][C:32]([NH:33]/[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:6]=[CH:7][CH:8]=[CH:9][CH:10]=3)=[CH:31][CH:30]=2)[CH2:25][CH2:26][CH2:27]1

Participants

3

Reactant 2

HCID 225694404-[(Azetidin-1-yl)methyl]anilineHCID 537348873-(1-Ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone

Product 1

HCID 178517258HCID 178517258, compound

Procedure

Prepared analogously to Example 89 by reacting 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone with 4-(azetidin-1-yl-methyl)-aniline.

Workup

  1. customPrepared analogously to Example 89

Sources & evidence

ORD record
ord-611cf589768e49f490a494c2b4df9255
Source dataset
uspto-grants-2005_02
Patent number
US06855710B2

Reaction notes

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