Hydrochloric Acid → HCID 22119903, compound
Reaction equation
[CH3:1][N:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][C:5](=[O:12])[N:4]([C:13]2[CH:14]=[CH:15][C:16]3[S:20][N:19]=[C:18]([CH2:21][C:22]([O:24]CC)=[O:23])[C:17]=3[CH:27]=2)[C:3]1=[O:28].Cl>ClCCCl>[CH3:1][N:2]1[C:7]([C:8]([F:9])([F:10])[F:11])=[CH:6][C:5](=[O:12])[N:4]([C:13]2[CH:14]=[CH:15][C:16]3[S:20][N:19]=[C:18]([CH2:21][C:22]([OH:24])=[O:23])[C:17]=3[CH:27]=2)[C:3]1=[O:28]Participants
4
Procedure
A mixture of ethyl 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-acetate (0.600 g), 10% hydrochloric acid (20.0 mL), and 1,2-dichloroethane (2.00 mL) is boiled for 30 minutes while allowing the 1,2-dichloroethane to evaporate, cooled, and poured onto ice. The resultant aqueous mixture is filtered to obtain a solid. The solid is washed with water and air-dried to give the title product as a white solid (0.550 g, mp 240-242° C.).
Workup
- customto evaporate
- temperaturecooled
- additionpoured onto ice
- filtrationThe resultant aqueous mixture is filtered
- customto obtain a solid
- washThe solid is washed with water
- customair-dried
Sources & evidence
- ORD record
- ord-91a662af98054948bd33ff86650e14fb
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06156700
Reaction notes
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