Methylamine → HCID 136377095, compound
Reaction equation
C[O:2][C:3]([C:5]1[N:6]=[C:7]([CH2:13][C:14]2[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:17]=[CH:16][C:15]=2[Br:24])[NH:8][C:9](=[O:12])[C:10]=1[OH:11])=O.[CH3:25][NH2:26]>C1COCC1>[CH3:25][NH:26][C:3]([C:5]1[N:6]=[C:7]([CH2:13][C:14]2[CH:19]=[C:18]([C:20]([F:21])([F:22])[F:23])[CH:17]=[CH:16][C:15]=2[Br:24])[NH:8][C:9](=[O:12])[C:10]=1[OH:11])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound was prepared according to the same procedure as in Example 21 using 2-(2-bromo-5-trifluoromethyl-benzyl)-5-hydroxy-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid methyl ester (0.080 g; 0.197 mmol) and 2M methylamine solution in THF (1 ml). This provided the title product as an off-white solid (0.043 g; 53%). LCMS: m/z=427 (MH+).
Workup
- customThe compound was prepared
Sources & evidence
- ORD record
- ord-8d6edd145af34fe2858946a075ac467f
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921388B2
Reaction notes
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