Hydrochloric Acid → HCID 67529179, compound
Reaction equation
[CH:1]1([CH:4]([NH:10]S(C(C)(C)C)=O)[CH2:5][C:6]([OH:9])([CH3:8])[CH3:7])[CH2:3][CH2:2]1.[ClH:17].O1CCOCC1>CO>[Cl-:17].[CH:1]1([CH:4]([NH3+:10])[CH2:5][C:6]([OH:9])([CH3:8])[CH3:7])[CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of N-(1-cyclopropyl-3-hydroxy-3-methylbutyl)-2-methylpropane-2-sulfinamide (0.56 g, 2.26 mmol) in MeOH (1.2 mL) was added 4 N HCl in dioxane (1.1 mL, 4.4 mmol). The reaction mixture was left to stir for 30 min, concentrated, and dried under high-vacuum to give the title compound. 1H NMR (600 MHz, CD3SOCD3) δ 7.75 (br s, 3H); 2.54 (m, 1H); 1.77 (dd, 1H); 1.65 (dd, 1H); 1.19 (s, 3H); 1.14 (s, 3H); 0.96 (m, 1H); 0.53 (m, 3H); 0.26 (m, 1H).
Workup
- waitThe reaction mixture was left
- concentrationconcentrated
- customdried under high-vacuum
Sources & evidence
- ORD record
- ord-d591d46e96c14a22bb3fa0d2d7ba46ad
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08431569B2
Reaction notes
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