Benzyl Bromide → HCID 54352100, compound
Reaction equation
Cl.[C:2]([NH:5][C@@H:6]1[CH2:10][NH:9][C@@H:8]([CH3:11])[CH2:7]1)(=[O:4])[CH3:3].C(N(CC)CC)C.[CH2:19](Br)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(Cl)Cl>[C:2]([NH:5][C@@H:6]1[CH2:10][N:9]([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C@@H:8]([CH3:11])[CH2:7]1)(=[O:4])[CH3:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
(2S,4S)-4-acetamido-2-methylpyrrolidine hydrochloride from the previous step is suspended in methylene chloride, triethylamine and benzyl bromide are added and the mixture heated at reflux. The product is obtained after washing and evaporation of the solvent.
Workup
- temperaturethe mixture heated
- temperatureat reflux
- customThe product is obtained
- washafter washing
- customevaporation of the solvent
Sources & evidence
- ORD record
- ord-baa17c0b8e6348348efaf0505fc733aa
- Source dataset
- uspto-grants-1994_06
- Patent number
- US05318965
Reaction notes
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