Water → HCID 68777436, compound
Reaction equation
FC(F)(F)C(O)=O.[O:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([NH:17][C:18]([N:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)=[O:19])=[N:9]1.C(N(CC)CC)C.[O:33]1[CH:37]=[CH:36][CH:35]=[C:34]1[C:38](Cl)=[O:39].O>O1CCCC1>[O:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([NH:17][C:18]([N:20]2[CH2:25][CH2:24][N:23]([C:38]([C:34]3[O:33][CH:37]=[CH:36][CH:35]=3)=[O:39])[CH2:22][CH2:21]2)=[O:19])=[N:9]1Participants
6
Procedure
To a solution of N-1,2-benzisoxazol-3-ylpiperazine-1-carboxamide trifluoroacetate (200 mg, 0.555 mmol) and triethylamine (0.309 ml, 2.22 mmol) in tetrahydrofuran (4 ml) was added 2-furoyl chloride (0.0821 ml, 0.833 mmol) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured to water and extracted with ethyl acetate. The extract was washed with water, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and ethyl acetate to give 100 mg (52.9%) of the desired product as a solid.
Workup
- temperaturecooling
- extractionextracted with ethyl acetate
- washThe extract was washed with water
- distillationthe solvent was distilled off under reduced pressure
- customThe residue was recrystallized from a mixed solvent of hexane and ethyl acetate
Sources & evidence
- ORD record
- ord-05eb90c7f03747ac96aa33b008354163
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07851473B2
Reaction notes
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