Benzyl Bromide → methyl 3-[N-(benzyl)-N-(diphenylmethyl)aminosulfonyl]-2(R)-methylpropionate
Reaction equation
[C:1]1([CH:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[NH:8][S:9]([CH2:12][C@H:13]([CH3:18])[C:14]([O:16][CH3:17])=[O:15])(=[O:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O-])([O-])=O.[K+].[K+].[CH2:31](Br)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>CN(C=O)C>[CH2:31]([N:8]([CH:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[S:9]([CH2:12][C@H:13]([CH3:18])[C:14]([O:16][CH3:17])=[O:15])(=[O:10])=[O:11])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 100 mL round bottom flask equipped with magnetic stir bar and N2 inlet was charged with 1.11 g of methyl 3-[N-(diphenylmethyl)aminosulfonyl]-2(R)-methylpropionate, 447 mg K2CO3, 347 mL benzyl bromide in 20 mL DMF. The reaction was stirred overnight, concentrated in vacuo and partioned between ethyl acetate and water. The organic phase was washed with brine, dried and concentrated in vacuo to 1.2 g of a clear oil. Flash chromatography on silica gel (30% ethyl acetate/hexanes) afforded 730 mg of methyl 3-[N-(benzyl)-N-(diphenylmethyl)aminosulfonyl]-2(R)-methylpropionate. HRMS (M+Li): calcd. 444.1821, obs 444.1865.
Workup
- customA 100 mL round bottom flask equipped with magnetic stir bar and N2 inlet
- concentrationconcentrated in vacuo
- washThe organic phase was washed with brine
- customdried
- concentrationconcentrated in vacuo to 1.2 g of a clear oil
Sources & evidence
- ORD record
- ord-5a6766a174334029ae46a34953ff95d6
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06384036B1
Reaction notes
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