Ammonium Chloride → HCID 89704796, compound
Reaction equation
[CH2:1]([C:4]1([S:7]([N:10]2[C:14]3=[CH:15][C:16]4[S:20][CH:19]=[N:18][C:17]=4[C:21]([F:22])=[C:13]3[N:12]([C:23]3[CH:28]=[CH:27][C:26]([Br:29])=[CH:25][C:24]=3[Cl:30])C2=O)(=[O:9])=[O:8])[CH2:6][CH2:5]1)[CH:2]=[CH2:3].C[Si](C)(C)[O-].[K+].[NH4+].[Cl-]>C1COCC1>[CH2:1]([C:4]1([S:7]([NH:10][C:14]2[C:13]([NH:12][C:23]3[CH:28]=[CH:27][C:26]([Br:29])=[CH:25][C:24]=3[Cl:30])=[C:21]([F:22])[C:17]3[N:18]=[CH:19][S:20][C:16]=3[CH:15]=2)(=[O:9])=[O:8])[CH2:6][CH2:5]1)[CH:2]=[CH2:3]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 7-((1-allylcyclopropyl)sulfonyl)-5-(4-bromo-2-chlorophenyl)-4-fluoro-5H-imidazo[4′,5′:4,5]benzo[1,2-d]thiazol-6(7H)-one (60 mg, 0.111 mmol) in THF (5 mL) was added potassium trimethylsilanolate (15 mg, 0.111 mmol). The mixture was stirred at room temperature for 1 h and treated with saturated NH4Cl (aq.). The aqueous layer was extracted with ethyl acetate (10 mL×2). The combined organic phase was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give a residue, which was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate, 5:1-3:1, v/v) to give the product as a white solid (50 mg, 87.5% yield). 1H NMR (400 MHz, CDCl3) δ 8.65 (s, 1H), 7.98 (s, 1H), 7.90 (d, 1H), 7.76 (d, 1H), 7.45 (m, 1H), 6.80 (s, 1H), 6.63 (s, 1H), 5.75-5.60 (m, 1H), 5.03 (m, 2H), 2.92-2.81 (m, 1H), 2.12-2.01 (m, 1H), 1.93-1.85 (m, 2H), 1.20-1.11 (m, 2H).
Workup
- extractionThe aqueous layer was extracted with ethyl acetate (10 mL×2)
- washThe combined organic phase was washed with brine (20 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto give a residue, which
- customwas purified by flash chromatography on silica gel (petroleum ether/ethyl acetate, 5:1-3:1
Sources & evidence
- ORD record
- ord-ac7c69ae8176407e9d20c05e578de44f
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290468B2
Reaction notes
Loading…