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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872047Generated: October 30, 2026

Chlorosuccinimide → HCID 59494548, compound

https://huagongshe.com/reaction/872047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 57763153HCID 57763153—
SolventDichloromethaneHCID 6344—
ProductHCID 59494548HCID 59494548114.4%

Reaction Steps

N-Chlorosuccinimide (514 mg) was added to a solution of tert-butyl 1H-pyrrolo[3,2-c]pyridin-6-carboxylate (800 mg) in dichloromethane (16 ml) at room temperature and the mixture was stirred at the room temperature for 3 hours. The reaction mixture was concentrated in vacuo and the resulted residue was dissolved in tetrahydrofuran. The organic layer was washed with saturated brine, dried over sodium sulfate and concentrated in vacuo to give a crude product of tert-butyl 3-chloro-1H-pyrrolo[3,2-c]pyridin-6-carboxylate (1.06 g) as an orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-90395f72db4a4983bcbbadcc6e1f18b6
Source noteuspto-grants-2015_03