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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040420Generated: October 31, 2026

Pyridine → 3-Benzothiazol-2-yl-3,5-dichloro-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/2040420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-oneHCID 57517750—
SolventDichloromethaneHCID 6344—
Product3-Benzothiazol-2-yl-3,5-dichloro-1,3-dihydroindol-2-oneHCID 57517751—

Reaction Conditions

Temperature0 °C

Reaction Steps

Pyridine (0.57 ml) and thionyl chloride (0.42 ml) were successively added to an ice-cooled solution of the intermediate from Step A (1.27 g, 4.0 mmol) in dichloromethane (40 ml). The reaction mixture was stirred at 0° C. for 1 h and then saturated ammonium chloride solution was added. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude intermediate was rapidly employed without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-c9df193f59ab4383bc2423c97194d810
Source noteuspto-grants-2013_11