4-(Trifluoromethyl)benzylamine → HCID 54694301, compound

HRID 1822692Notes

Reaction equation

HRID 1822692 reaction equation
C(O[C:4]([C:6]1[N:7]=[C:8]([C:15]2[C:20]([F:21])=[CH:19][CH:18]=[CH:17][C:16]=2[F:22])[N:9]([CH3:14])[C:10](=[O:13])[C:11]=1[OH:12])=[O:5])C.[F:23][C:24]([F:34])([F:33])[C:25]1[CH:32]=[CH:31][C:28]([CH2:29][NH2:30])=[CH:27][CH:26]=1>>[F:23][C:24]([F:33])([F:34])[C:25]1[CH:32]=[CH:31][C:28]([CH2:29][NH:30][C:4]([C:6]2[N:7]=[C:8]([C:15]3[C:16]([F:22])=[CH:17][CH:18]=[CH:19][C:20]=3[F:21])[N:9]([CH3:14])[C:10](=[O:13])[C:11]=2[OH:12])=[O:5])=[CH:27][CH:26]=1

Participants

3

Reactant 2

HCID 768044-(Trifluoromethyl)benzylamineHCID 546914342-(2,6-Difluoro-phenyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid ethyl ester

Product 1

HCID 54694301HCID 54694301, compound

Procedure

Prepared according to the procedure described for example 2 from 2-(2,6-difluoro-phenyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid ethyl ester (31 mg, 0.1 mmol) and 4-trifluoromethylbenzylamine (88 mg, 0.5 mmol). The title product was obtained as an off-white solid (38.6 mg, 88% yield). 1HNMR (500 MHz, CDCl3) δ: 12.18 (1H, s), 7.88 (1H, t, J=4.58), 7.60 (2H, d, J=8.24 Hz), 7.53–7.47 (1H, m), 7.43 (2H, d J=8.24 Hz), 7.05 (2H, dd, J=8.24, 7.32 Hz), 4.65 (2H, d, J=6.41 Hz), 3.42 (3H, s). HRMS (ESI) calcd for C20H13F5N3O3 (M−H): 438.0877; found: 438.0878.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-ed88ccb1d7f3411e9a8585351b8261ea
Source dataset
uspto-grants-2006_05
Patent number
US07037908B2

Reaction notes

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