Hydrogen chloride-ethyl acetate → HCID 178448897, compound
Reaction equation
[F:1][C:2]([F:33])([F:32])[C:3]1[CH:27]=[C:26]([C:28]([F:31])([F:30])[F:29])[CH:25]=[CH:24][C:4]=1[CH2:5][N:6]1[CH2:11][CH2:10][CH:9](/[CH:12]=[C:13]2/[C:14]([NH:19][CH:20]([CH3:23])[C:21]#[CH:22])=[N:15][C:16](=[O:18])[S:17]/2)[CH2:8][CH2:7]1.[ClH:34].C(OCC)(=O)C>C(OCC)(=O)C>[ClH:34].[F:33][C:2]([F:1])([F:32])[C:3]1[CH:27]=[C:26]([C:28]([F:30])([F:31])[F:29])[CH:25]=[CH:24][C:4]=1[CH2:5][N:6]1[CH2:7][CH2:8][CH:9](/[CH:12]=[C:13]2/[C:14]([NH:19][CH:20]([CH3:23])[C:21]#[CH:22])=[N:15][C:16](=[O:18])[S:17]/2)[CH2:10][CH2:11]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (5Z)-5-({1-[2,4-bis(trifluoromethyl)benzyl]piperidin-4-yl}methylidene)-4-[(1-methylprop-2-yn-1-yl)amino]-1,3-thiazol-2(5H)-one (980 mg) in ethyl acetate (10 mL) was added 4N hydrogen chloride/ethyl acetate (0.50 mL) solution, and the precipitate was collected by filtration to give the title compound (635 mg).
Workup
- filtrationthe precipitate was collected by filtration
Sources & evidence
- ORD record
- ord-7afe5309cd9b4f559ede676fb344185d
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772277B2
Reaction notes
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