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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436755Generated: November 2, 2026

Triethylamine → HCID 57938714, compound

https://huagongshe.com/reaction/1436755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methoxyoxan-4-oneHCID 23533610—
ReactantHCID 86633368HCID 86633368—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 57938714HCID 57938714—

Reaction Steps

To a solution of (1R,3S)-3-isopropyl-3-({4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}carbonyl)cyclopentanamine bis(trifluoroacetate) (140 mg, 0.23 mmol), 3-methoxytetrahydro-4H-pyran-4-one (90 mg, 0.69 mmol) and triethylamine (0.096 mL, 0.69 mmol) in methylene chloride (10 mL) was added sodium triacetoxyborohydride (97 mg, 0.46 mmol). After being stirred at room temperature overnight, the reaction mixture was diluted with EtOAc and washed with saturated Na2CO3. The aqueous layer was extracted with EtOAc three times. The combined organic layers were dried (MgSO4), concentrated and purified on silica gel eluting with EtOAc to 1% Et3N/EtOAc affording 105 mg (92%) of the desired product. The product was separated by chiral HPLC to give two major isomers. MS calculated for C26H38F3N3O3: (M+H) 498; found 498.2 for both isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618970B2
Source datasetuspto-grants-2009_11
ORD IDord-c08fe81c298b4bc981ae0a30416333e0
Source noteuspto-grants-2009_11