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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599389Generated: November 4, 2026

Phenyl chloroformate → HCID 18928232, compound

https://huagongshe.com/reaction/1599389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Chloro-4-(pyridin-3-yl)-1,2,5-thiadiazoleHCID 10488164—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18928232HCID 18928232—

Reaction Conditions

Temperature-25 °C

Reaction Steps

A solution of cuprous iodide (0.40 g, 2 mmol) in dry THF (50 ml) was stirred under nitrogen for 10 min. A solution of 3-(3-chloro-1,2,5-thiadiazol-4-yl)pyridine (J.Med.Chem. 1992, 35, 2274-2283) (9.9 g, 50 mmol) in dry THF (150 ml) was added to the reaction, then cooled to -25° C. Phenylchloroformate (6.3 ml, 50 mmol) in THF (20 ml) was added slowly. The reaction mixture was stirred at -25° C. for 30 min., then allowed to warm to room temperature and stirred for another 2.5 h. The reaction mixture was cooled to -25° C. and methylmagnesium iodide (55 mmol in 20 ml ether) was added. The reaction mixture was stirred for 20 min., 20% NH4Cl(aq) (100 ml) was added and then extracted with ether (200 ml). The combined organic phases were washed with 20% NH4Claq :NH4OH (1:1) (50 ml), water (50 ml), 4N HCl (50 ml), water (50 ml) and brine (50 ml). The organic phases were dried and evaporated to give crude title compound. Purification on column chromatography, eluent: toluene, gave the title compound in 11.9 g (71%) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05741788
Source datasetuspto-grants-1998_04
ORD IDord-8895ac1867a144e688913d18474d7429
Source noteuspto-grants-1998_04