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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436776Generated: November 1, 2026

Triethylamine → 1-({(1S,3R)-1-Isopropyl-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]cyclopentyl}carbonyl)-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol

https://huagongshe.com/reaction/1436776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methoxyoxan-4-oneHCID 23533610—
Reactant1-{[(1S,3R)-3-amino-1-isopropylcyclopentyl]carbonyl}-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol hydrochlorideHCID 68930927—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
Product1-({(1S,3R)-1-Isopropyl-3-[(3-methoxytetrahydro-2H-pyran-4-yl)amino]cyclopentyl}carbonyl)-4-[2-(trifluoromethyl)phenyl]piperidin-4-olHCID 1164920558.5%
ProductAmmonium hydroxide methanolHCID 218945081%

Reaction Steps

To a solution of 1-{[(1S,3R)-3-amino-1-isopropylcyclopentyl]carbonyl}-4-[2-(trifluoromethyl) phenyl]piperidin-4-ol hydrochloride (50 mg, 0.1 mmol) , 3-methoxytetrahydro-4H-pyran-4-one (45 mg, 0.34 mmol) , and triethylamine (0.048 mL, 0.34 mmol) in methylene chloride (2 mL) was added sodium triacetoxyborohydride (0.073 g, 0.34 mmol). After being stirred overnight at room temperature, a saturated solution of NaHCO3 was added. The solution was extracted with methylene chloride three times. The combined extracts were dried (MgSO4), filtered, and concentrated. Purification by flash chromatography on silica gel (0-20% B over 15 min. Bottle A=1% NH4OH/2% MeOH/EtOAc, Bottle B=1% NH4OH/MeOH) afforded 15 mg of the desired product as an oil. MS calculated for C27H39F3N2O4:(M+H) 513; found 513.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618970B2
Source datasetuspto-grants-2009_11
ORD IDord-82726dea443749d9bbb60bf79f80a4e8
Source noteuspto-grants-2009_11