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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449739Generated: October 31, 2026

Pyridine → HCID 21477616, compound

https://huagongshe.com/reaction/1449739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantEthyl 5-amino-1H-indole-2-carboxylateHCID 10726872—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21477616HCID 21477616—

Reaction Steps

Ethyl 5-aminoindole-2-carboxylate (2.0 g) and pyridine (0.82 ml) are dissolved in 15 ml of methylene chloride and 10 ml of THF. Then the reaction is cooled to 0° and 3-chloropropanesulfonyl chloride (1.25 ml) is added and the reaction is allowed to slowly warm to 20°-25° and stir for 16 hr. Then the reaction is diluted with chloroform, washed with saturated aqueous sodium bicarbonate and saline. The organic layers are dried over anhydrous sodium sulfate and concentrated under reduced pressure. The product is dissolved in ethyl acetate and filtered through a plug of silica gel and crystallized from methanol, mp 195°-196°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599930
Source datasetuspto-grants-1997_02
ORD IDord-d9407e3ad9ee44beba7ce3f68d005fe4
Source noteuspto-grants-1997_02