Allylamine → HCID 39871266, compound
Reaction equation
[CH2:1]([NH2:4])[CH:2]=[CH2:3].[C:5](N1C=CN=C1)([N:7]1[CH:11]=[CH:10][N:9]=[CH:8]1)=[O:6]>ClCCl>[N:7]1([C:5]([NH:4][CH2:1][CH:2]=[CH2:3])=[O:6])[CH:11]=[CH:10][N:9]=[CH:8]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Allylamine (1.0 g, 17.5 mmol) was dissolved in dichloromethane (30 ml), 1,1′-carbonyldiimidazole (7.37 g, 15 mmol) was added, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound.
Workup
- customThe solvent was evaporated under reduced pressure
- customthe residue was partitioned between ethyl acetate and 1N hydrochloric acid
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-7aabe98ebef8407eb3ccd4cb183ea754
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346821B2
Reaction notes
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