Reaktion #357734

Reaktionsgleichung

triethylamine

1-[5-(trifluoromethyl)pyridin-3-yl]piperazine trihydrochloride

(1S,3R)-3-[(tert-butoxycarbonyl)amino]-1-isopropylcyclopentanecarboxylic acid

benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate

→

desired product

Ausbeute 170.5%

tert-Butyl [(1R,3S)-3-Isopropyl-3-({4-[5-(trifluoromethyl)pyridin-3-yl]piperazin-1-yl}carbonyl)cyclopentyl]carbamate

Ausbeute 170.5%

Lösungsmittel

methylene chloride

EtOAc

Reaktionsbedingungen

Aufarbeitung

1. 1
   WaschenThe solution was washed with saturated NaHCO3
2. 2
   Trocknendried (MgSO4)
3. 3
   Einengenconcentrated
4. 4
   SonstigeThe residue was purified by flash chromatography on silica gel (20% EtOAc/hexanes to 40% EtOAc/hexanes)

Vorschrift

To a solution of 1-[5-(trifluoromethyl)pyridin-3-yl]piperazine trihydrochloride (0.22 g, 0.23 mmol), (1S,3R)-3-[(tert-butoxycarbonyl)amino]-1-isopropylcyclopentanecarboxylic acid (0.18 g, 0.66 mmol) in methylene chloride (10 mL) was added benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (0.338 g, 0.764 mmol) followed by triethylamine (0.22 mL, 1.6 mmol). The mixture was stirred at room temperature overnight and diluted with EtOAc. The solution was washed with saturated NaHCO3, dried (MgSO4) and concentrated. The residue was purified by flash chromatography on silica gel (20% EtOAc/hexanes to 40% EtOAc/hexanes) to give 0.19 g (61%) of desired product. MS calculated for C24H35F3N4O3: (M+H) 485; found 485.2.

Quelle