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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52134Generated: October 25, 2026

Hydrochloric Acid → N,N-diethyl-3-(diethylthiocarbamoyloxy)-2-fluoronicotinamide

https://huagongshe.com/reaction/52134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethylcarbamoyl chlorideHCID 6916—
Reactant3-Diethylthiocarbamoyloxy-2-fluoropyridineHCID 19963242—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diethyl-3-(diethylthiocarbamoyloxy)-2-fluoronicotinamideHCID 1996324565%

Reaction Conditions

Temperature-10 °C

Reaction Steps

250 ml (400 mmol) of n-BuLi (1.6M in hexane) are added to a solution of 57.9 g (410 mmol) of TMP in 750 ml of THF at -10° C. After the mixture has been stirred for 1 hour at -10° C., a solution of 64 g (280 mmol) of 3-diethylthiocarbamoyloxy-2-fluoropyridine in 200 ml of THF is added dropwise at -78° C. in the course of 30 minutes. After the mixture has been stirred for 1 hour at -78° C., 81.4 g (600 mmol) of diethylcarbamoyl chloride are added in the course of 1 minute, the mixture is stirred at -78° C. for 2 hours and heated to -20° C., 130 ml of 3N HCl are added, and the mixture is diluted with 1 l of water and brought to pH 7. The organic phase is washed 3 times with water. The combined aqueous phases are extracted twice using Et2O, and the combined organic phases are washed twice with water, dried over Na2SO4 and concentrated in vacuo at 60° C.: 116 g of a brown oil. Chromatography (ethyl acetate/hexane 1:1) gives 60 g (65% ) of beige crystals of m.p. 87°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616590
Source datasetuspto-grants-1997_04
ORD IDord-88ddd8716b694fdaabf8855cf92a9544
Source noteuspto-grants-1997_04