Hydrochloric Acid → HCID 68780263, compound
Reaction equation
[C:1]1([C:7]2[N:8]=[C:9]([N:12]3[CH2:17][CH2:16][N:15]([C:18]([NH:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)=[O:19])[CH2:14][CH2:13]3)[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:27]>O1CCCC1.C(OCC)(=O)C>[ClH:27].[C:1]1([C:7]2[N:8]=[C:9]([N:12]3[CH2:17][CH2:16][N:15]([C:18]([NH:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)=[O:19])[CH2:14][CH2:13]3)[S:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 4-(4-phenyl-1,3-thiazol-2-yl)-N-pyridin-3-ylpiperazine-1-carboxamide (1.00 g, 2.74 mmol) in tetrahydrofuran (100 ml) was added a 4N solution of hydrogen chloride in ethyl acetate (20 ml) at room temperature. The mixture was stirred at room temperature for 2 hours and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of diethyl ether and methanol to obtain the desired product (1.09 g, 99.0%) as a solid.
Workup
- distillationthe solvent was distilled off under reduced pressure
- customThe residue was recrystallized from a mixed solvent of diethyl ether and methanol
Sources & evidence
- ORD record
- ord-c0bb8d5c76ba4bdcb4dc901cc139da7a
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07851473B2
Reaction notes
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