Ethanamine, 2,2,2-trifluoro- → HCID 71623152, compound
Reaction equation
CCN(C(C)C)C(C)C.[C:10]([O:14][C:15]([NH:17][CH2:18][C:19]([OH:21])=O)=[O:16])([CH3:13])([CH3:12])[CH3:11].C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[F:55][C:56]([F:60])([F:59])[CH2:57][NH2:58]>ClCCl>[C:10]([O:14][C:15](=[O:16])[NH:17][CH2:18][C:19](=[O:21])[NH:58][CH2:57][C:56]([F:60])([F:59])[F:55])([CH3:11])([CH3:12])[CH3:13]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
DIPEA (15 ml) is added to a solution of N-(tert-butoxycarbonyl)glycine (5.0 g), PYBOP (benzotriazol-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate, 16.3 g) and 2,2,2-trifluorethylamine (2.47 ml) in dichloromethane (48 ml). After 24 hours at room temperature, the reaction is quenched with water and extracted three times with dichloromethane. The combined organic phases are washed with HCl (2M), Na2CO3 (1M) and a saturated aqueous solution of NaCl, dried over MgSO4 and concentrated in vacuo. The crude product is purified by column chromatography (450 g) eluting with a mixture of ethyl acetate and hexane (2:3 to 3:2) to yield [(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-carbamic acid tert-butyl ester (3.89 g).
Workup
- customthe reaction is quenched with water
- extractionextracted three times with dichloromethane
- washThe combined organic phases are washed with HCl (2M), Na2CO3 (1M)
- dry with materiala saturated aqueous solution of NaCl, dried over MgSO4
- concentrationconcentrated in vacuo
- customThe crude product is purified by column chromatography (450 g)
- washeluting with a mixture of ethyl acetate and hexane (2:3 to 3:2)
Sources & evidence
- ORD record
- ord-d532443417c2454fbe701d226f1fec14
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08653116B2
Reaction notes
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