HCID 59411295, compound → HCID 59411327, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[N:14]([CH2:15][C:16]3[CH:17]=[C:18]([CH:26]=[CH:27][CH:28]=3)[C:19]([O:21]C(C)(C)C)=[O:20])[C:13](=[O:29])[N:12]([C:30]3[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:39])([F:38])[F:37])[CH:31]=3)[C:11]([CH3:40])=[C:10]2[C:41]([C:43]2[O:44][CH:45]=[CH:46][CH:47]=2)=[O:42])=[CH:5][CH:4]=1)#[N:2]>FC(F)(F)C(O)=O>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[N:14]([CH2:15][C:16]3[CH:17]=[C:18]([CH:26]=[CH:27][CH:28]=3)[C:19]([OH:21])=[O:20])[C:13](=[O:29])[N:12]([C:30]3[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:39])([F:38])[F:37])[CH:31]=3)[C:11]([CH3:40])=[C:10]2[C:41]([C:43]2[O:44][CH:45]=[CH:46][CH:47]=2)=[O:42])=[CH:5][CH:4]=1)#[N:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl 3-{[6-(4-cyanophenyl)-5-(2-furoyl)-4-methyl-2-oxo-3-[3-(trifluoromethyl)phenyl]-3,6-dihydropyrimidin-1(2H)-yl]methyl}benzoate (Example 43) (50 mg, 0.078 mmol) is dissolved in trifluoroacetic acid (2 ml). After 15 minutes stirring, the solution is concentrated in vacuo and the residue is purified by preparative HPLC (RP18 column; eluent: acetonitrile/water 10:90→90:10).
Workup
- concentrationthe solution is concentrated in vacuo
- customthe residue is purified by preparative HPLC (RP18 column; eluent: acetonitrile/water 10:90→90:10)
Sources & evidence
- ORD record
- ord-f032eba0972c40b7b0a5c4043ef7ef45
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893073B2
Reaction notes
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