Hexane → HCID 68489879, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:10][C:9](=[O:11])[O:8][C:7]([CH2:16][CH2:17][NH:18][S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=3)(=[O:21])=[O:20])([C:12]([F:15])([F:14])[F:13])[C:6]=2[CH:28]=1.CCCCCC>CC(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:10][C:9](=[O:11])[O:8][C@@:7]([CH2:16][CH2:17][NH:18][S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=3)(=[O:21])=[O:20])([C:12]([F:15])([F:14])[F:13])[C:6]=2[CH:28]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-{2-[6-chloro-2-oxo-4-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-4-yl]ethyl}pyridine-2-sulfonamide was subjected to optical resolution by HPLC (Chiralpack AD-H, 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-94ee66c02d9b4db893180e3723c84bf1
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314094B2
Reaction notes
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