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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580348Generated: October 30, 2026

Chlorosuccinimide → HCID 14232132, compound

https://huagongshe.com/reaction/580348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 14232111HCID 14232111—
ReactantSodium BisulfiteHCID 23665763—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14232132HCID 1423213264.6%

Reaction Steps

To a solution of N-(4-pyridinyl)-N-(1H-pyrrol-1-yl)carbamic acid ethyl ester (9 g) in 100 ml of anhydrous tetrahydrofuran warmed to 50° was slowly dropped a solution of N-chlorosuccinimide (5.2 g) in 75 ml of anhydrous tetrahydrofuran. After stirring seven hours at 50°, the reaction mixture was cooled, stirred with an aqueous solution of sodium bisulfite and extracted with ethyl acetate. The organic extract was washed with water and saturated sodium chloride and thereafter dried over anhydrous magnesium sulfate, filtered and evaporated to 11.5 g of an oil. This oil was purified by HPLC (silica, 20% ethyl acetate in dichloromethane) to give 3.8 g of the desired product as a solid. This material was converted to the hydrochloride salt and twice recrystallized from isopropanol-ether to give 3.3 g of crystals, d 139°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752610
Source datasetuspto-grants-1988_06
ORD IDord-247e6470c3b340daa4ba159a732ff010
Source noteuspto-grants-1988_06