Triethylamine → HCID 11557656, compound
Reaction equation
Br.[NH2:2][C@H:3]([C:8]([N:10]1[CH2:17][CH2:16][CH2:15][C@H:11]1[C:12]([NH2:14])=[O:13])=[O:9])[CH2:4][CH:5]([CH3:7])[CH3:6].C(N(CC)CC)C>CN(C=O)C>[NH2:2][C@H:3]([C:8]([N:10]1[CH2:17][CH2:16][CH2:15][C@H:11]1[C:12]([NH2:14])=[O:13])=[O:9])[CH2:4][CH:5]([CH3:6])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -10 °C
Procedure
L-Leucyl-L-prolinamide hydrobromide (517 mg) was dissolved in DMF (1.5 ml), to which was added triethylamine (0.35 ml) under cooling at -10° C. The mixture was stirred for 10 minutes under ice-cooling and the resultant precipitate was filtered off to give L-leucyl-L-prolinamide in DMF solution, which was immediately used for the next reaction.
Workup
- temperaturecooling
- filtrationthe resultant precipitate was filtered off
Sources & evidence
- ORD record
- ord-c7f6d573d3294e99a72d387976fe8093
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05151497
Reaction notes
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