Triethylamine → HCID 178462003, compound
Reaction equation
[CH3:1][N:2]([CH3:8])[C:3](=[O:7])[C@H:4]([CH3:6])[NH2:5].C(N(CC)CC)C.S=[C:17]1[CH2:21][S:20][C:19](=[O:22])[NH:18]1>C(O)C>[CH3:1][N:2]([CH3:8])[C:3](=[O:7])[C@H:4]([CH3:6])[NH:5][C:17]1[CH2:21][S:20][C:19](=[O:22])[N:18]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the crude product containing N,N-dimethylalaninamide obtained in C) and triethylamine (2 mL) in ethanol (20 mL) was added 4-thioxothiazolidin-2-one (1998 mg) at room temperature. The reaction mixture was stirred at room temperature overnight, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (960 mg).
Workup
- customthe solvent was evaporated under reduced pressure
- customThe residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane)
Sources & evidence
- ORD record
- ord-798cc931a40440d89e28e2f2f798ef50
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772277B2
Reaction notes
Loading…