Triethylamine → HCID 59608173, compound
Reaction equation
Cl.[NH2:2][C@H:3]([CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:15][CH:14]=1)[CH2:4][C@@H:5]([CH3:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7].Cl[C:26](=[O:32])[C:27]([O:29][CH2:30][CH3:31])=[O:28].C(N(CC)CC)C>CN(C=O)C>[C:16]1([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:15]=[CH:14][C:13]([CH2:12][C@@H:3]([NH:2][C:26](=[O:32])[C:27]([O:29][CH2:30][CH3:31])=[O:28])[CH2:4][C@@H:5]([CH3:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:18][CH:17]=1Participants
5
Procedure
To a solution of (2R,4S)-ethyl 4-amino-5-(biphenyl-4-yl)-2-methylpentanoate hydrochloride salt (1 g, 2.87 mmol) in DMF (10 mL) is added TEA (0.42 mL, 3.02 mmol) followed by ethyl 2-chloro-2-oxoacetate (392 mg, 2.87 mmol). The crude is stirred at it for 1 hr. To the crude is added an additional 0.2 ml of ethyl 2-chloro-2-oxoacetate followed by triethylamine (1.26 mL, 9.06 mmol). The crude is quenched with water and diluted in EtOAc. The organic layer is washed with brine, dried over MgSO4, filtered, and concentrated. The crude is purified via flash chromatography using 30% EtOAc/heptane to 50% EtOAc/heptane to give (2R,4S)-ethyl 5-(biphenyl-4-yl)-4-(2-ethoxy-2-oxoacetamido)-2-methylpentanoate (970 mg).
Workup
- customThe crude is quenched with water
- additiondiluted in EtOAc
- washThe organic layer is washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude is purified via flash chromatography
Sources & evidence
- ORD record
- ord-0e3593aba04e429791e78340908b2163
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263629B2
Reaction notes
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