Dibenzylamine → HCID 24810021, compound

HRID 1446200Notes

Reaction equation

HRID 1446200 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[CH:10][C:9]=2[C:13]([OH:15])=O)=[CH:4][CH:3]=1.[CH2:16]([NH:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:24]([N:23]([CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:13]([C:9]1[CH:10]=[N:11][O:12][C:8]=1[C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=1)=[O:15])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

Participants

3

Reactant 2

HCID 7656DibenzylamineHCID 228317065-(p-Tolyl)isoxazole-4-carboxylic acid

Product 1

HCID 24810021HCID 24810021, compound

Procedure

The title compound was prepared from 5-(4-methylphenyl)isoxazole-4-carboxylic acid (10.2 mg, 0.050 mmol) and dibenzylamine (11.8 mg, 0.060 mmol) as described in synthetic method B and thereafter purified by preparative HPLC method B to give a solid (2.6 mg). Calcd for C25H22N2O2: 382.1681, found 382.1684.

Workup

  1. custompurified by preparative HPLC method B

Sources & evidence

ORD record
ord-1d6888c519c5494da87756482281ce1b
Source dataset
uspto-grants-2010_02
Patent number
US07666888B2

Reaction notes

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