Hexane → HCID 68489309, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[NH:6][C:5]2([CH2:17][NH:18][C:19](=[O:27])[C:20]1[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=1)[C:13]([F:16])([F:15])[F:14].CCCCCC>CC(O)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[NH:6][C@@:5]2([CH2:17][NH:18][C:19](=[O:27])[C:20]1[CH:21]=[CH:22][C:23]([F:26])=[CH:24][CH:25]=1)[C:13]([F:16])([F:14])[F:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-{[6-chloro-2-oxo-4-(trifluoromethyl)-1,2,3,4-tetrahydroquinazolin-4-yl]methyl}4-fluorobenzamide was subjected to optical resolution by HPLC (Chiralpack AD-H, n-hexane:2-propanol=3:1), and a fraction eluted at a later time was concentrated, whereby the objective compound was obtained.
Workup
- washa fraction eluted at a later time
- concentrationwas concentrated
- customwhereby the objective compound was obtained
Sources & evidence
- ORD record
- ord-dbe9a8c2cbdf4b6494ae9265cad0653e
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314094B2
Reaction notes
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