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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22748Generated: October 29, 2026

Chlorosuccinimide → HCID 22591558, compound

https://huagongshe.com/reaction/22748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant3-Methoxy-6-(indole-2-sulfenyl)-pyridazineHCID 12071764—
SolventMethanolHCID 887—
ProductHCID 22591558HCID 2259155840%

Reaction Steps

A mixture of 3-methoxy-6-(indole-2-sulfenyl)-pyridazine) (2.92 mmol, 750 mg), N-chloro-succinimide (2.92 mmol, 390 mg) and methanol (15 mL) was stirred overnight at room temperature. Excess methanol was removed and the residue was extracted with EtOAc (3×10 mL). The EtOAc extract was collected, dried, filtered and evaporated to dryness to obtain a residue, which was purified by silica gel chromatography (eluent:hexanes:EtOAc::19:5) to yield 3-methoxy-6-(3-chloro-indole-2-sulfenyl)-pyridazine (40%, 338 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849629B2
Source datasetuspto-grants-2005_02
ORD IDord-573ba61d162e49dd86ea5bb52ca15369
Source noteuspto-grants-2005_02