Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424538Generated: November 2, 2026

(Diethylamino)sulfur trifluoride → N-Cyclopropyl-N-[1-(2-fluoro-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide

https://huagongshe.com/reaction/1424538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
ReactantN-Cyclopropyl-N-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 86709612—
SolventDichloromethaneHCID 6344—
ProductN-Cyclopropyl-N-[1-(2-fluoro-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 73053140—

Reaction Steps

Diethylaminosulfur trifluoride (57 μL) is added drop wise to N-cyclopropyl-N-[1-(2-hydroxy-2-methyl-propyl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide (83 mg) in dry dichloromethane (12 mL) at −78° C. and the reaction mixture is stirred at this temperature for 2 h. The mixture is poured on aqueous NaHCO3 solution (15 mL) and the aqueous phase is extracted with dichloromethane. The combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo. The solid residue is triturated with diisopropyl ether, filtered off, and dried to give the title compound. LC (method 2): tR=1.10 min; Mass spectrum (ESI+): m/z =386 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927726B2
Source datasetuspto-grants-2015_01
ORD IDord-f7f351e83b474d7882c82086ee1d49ac
Source noteuspto-grants-2015_01