Hydrochloric Acid → HCID 86688426, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:10][S@](C(C)(C)C)=O)[CH3:9])=[C:4]([C:17]([F:20])([F:19])[F:18])[CH:3]=1.Cl.O1CCOCC1.C(OCC)C>CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH2:10])[CH3:9])=[C:4]([C:17]([F:18])([F:19])[F:20])[CH:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (S)—N—((R)-1(4-chloro-2-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide (14.6 g, 44.5 mmol) in methanol (25 mL) was added a solution of hydrochloric acid in p-dioxane (4.0 M in p-dioxane, 22.3 mL, 89.1 mmol), and the reaction was stirred at room temperature for 30 min. Diethyl ether was then added (400 mL) and the slurry was stirred for 10 min. The solid was collected by filtration, and washed with diethyl ether (2×200 mL). The solid was then dissolved in 5 M aqueous sodium hydroxide solution, and extracted with dichloromethane (2×100 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was used without further purification (7.8 g, 34.9 mmol, 79%, >96% ee, determined by Mosher's method).
Workup
- stirringthe slurry was stirred for 10 min
- filtrationThe solid was collected by filtration
- washwashed with diethyl ether (2×200 mL)
- dissolutionThe solid was then dissolved in 5 M aqueous sodium hydroxide solution
- extractionextracted with dichloromethane (2×100 mL)
- dry with materialThe combined organic layers were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude product was used without further purification (7.8 g, 34.9 mmol, 79%, >96% ee, determined by Mosher's method)
Sources & evidence
- ORD record
- ord-189e55ad64934cb7973c0217fb523914
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150550B2
Reaction notes
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