Ethanamine, 2,2,2-trifluoro- → HCID 71623152, compound

HRID 242403Notes

Reaction equation

HRID 242403 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

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

  1. customthe reaction is quenched with water
  2. extractionextracted three times with dichloromethane
  3. washThe combined organic phases are washed with HCl (2M), Na2CO3 (1M)
  4. dry with materiala saturated aqueous solution of NaCl, dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customThe crude product is purified by column chromatography (450 g)
  7. 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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