Dimethyl Sulfoxide → HCID 67407708, compound
Reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[OH:11][CH:12]([C:24]([CH3:27])([CH3:26])[CH3:25])[CH2:13][CH:14]1[O:18][N:17]=[C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:15]1.C(N(CC)CC)C>ClCCl>[CH3:26][C:24]([CH3:25])([CH3:27])[C:12](=[O:11])[CH2:13][CH:14]1[O:18][N:17]=[C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:15]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
A solution of DMSO (3.94 mL, 55.6 mmol) in dichloromethane (90 mL) at −78° C. was treated dropwise with oxalyl chloride (20.8 mL, 2 M in dichloromethane), stirred at −78° C. for 15 minutes, treated with a solution of the product from Example 115B (6.76 g, 27.8 mmol) in dichloromethane (230 mL) over 10 minutes, stirred at −78° C. for 20 minutes, treated dropwise with triethylamine (16.7 mL, 119.5 mmol) at −78° C., and after 10 minutes the reaction was warmed to 0° C., and stirred for an additional 10 minutes. The reaction mixture was quenched with water and partitioned between dichloromethane and water. The organic phase was washed with brine and dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel eluting with 5% ethyl acetate in chloroform to give the title compound (4.9 g, 73% yield).
Workup
- stirringstirred at −78° C. for 20 minutes
- temperatureafter 10 minutes the reaction was warmed to 0° C.
- stirringstirred for an additional 10 minutes
- customThe reaction mixture was quenched with water
- custompartitioned between dichloromethane and water
- washThe organic phase was washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was chromatographed on silica gel eluting with 5% ethyl acetate in chloroform
Sources & evidence
- ORD record
- ord-cdcc183fd6fc4ca2bdbdbc1b597656d1
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834043B2
Reaction notes
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