Ethanol → HCID 21697690, compound
Reaction equation
[O:1]=[S:2]1(=[O:16])[CH:6]([F:7])[C:5]2[C:8]([Cl:15])=[CH:9][CH:10]=[C:11]([N+:12]([O-])=O)[C:4]=2[NH:3]1.[Sn](Cl)Cl.[CH2:20](O)C>>[O:1]=[S:2]1(=[O:16])[C:6]([F:7])([CH3:20])[C:5]2[C:8]([Cl:15])=[CH:9][CH:10]=[C:11]([NH2:12])[C:4]=2[NH:3]1Participants
4
Procedure
To the solution of 1,3-dihydro-2,2-dioxo-4-chloro-3-fluoro-7-nitro-2,1-benzisothiazole (100 mg, 0.4 mmol) in ethanol (10 ml), Tin (II) chloride (443 mg, 2.0 mmol) was added. The reaction mixture was stirred at room temperature for about 16 hours. Then all solvent was evaporated. Chromatography of the residue on silica gel (50% Ethyl acetate/Hexane) gave desired product (43 mg, 47%). EI-MS m/z 237.2 (M+).
Workup
- customThen all solvent was evaporated
Sources & evidence
- ORD record
- ord-b5333b8af1b3464ca4cb84fe878cbadc
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06297265B2
Reaction notes
Loading…