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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270584Generated: October 31, 2026

Triethylamine → N-[(1R,3S)-3-Isopropyl-3-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methyltetrahydro-2H-pyran-4-amine

https://huagongshe.com/reaction/270584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methyloxan-4-oneHCID 14170926—
Reactant(1R,3S)-3-isopropyl-3-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentanamine dihydrochlorideHCID 68597226—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-[(1R,3S)-3-Isopropyl-3-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentyl]-3-methyltetrahydro-2H-pyran-4-amineHCID 1165597279.7%

Reaction Steps

To a solution of (1R,3S)-3-isopropyl-3-(4-[6-(trifluoromethyl)pyridin-2-yl]piperazin-1-ylcarbonyl)cyclopentanamine dihydrochloride (120 mg, 0.26 mmol), 3-methyltetrahydro-4H-pyran-4-one (75 mg, 0.66 mmol), triethylamine (0.15 mL, 1.0 mmol) in methylene chloride (8 mL) was added sodium triacetoxyborohydride (0.17 g, 0.79 mmol). After being stirred at room temperature overnight, the reaction mixture was diluted with water and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography (ethyl acetate to EtOAc/Et3N=10:0.1) to yield the desired product (100 mg, 79%). LCMS calculated for C25H38F3N4O2: (M+1) 483.2; found 483.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449467B2
Source datasetuspto-grants-2008_11
ORD IDord-4a803c9c6c7741b29e40a30af5b9f2fd
Source noteuspto-grants-2008_11