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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601756Generated: October 29, 2026

Benzothiazole → 3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/601756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Benzothiazol-2-yl-5-chloro-3-hydroxy-1,3-dihydroindol-2-oneHCID 5751775070.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 1.6 M solution of n-butyllithium in hexane (35 ml, 56 mmol) was added dropwise to a solution of benzothiazole (6.2 ml, 56 mmol) in THF (100 ml) at −78° C. After stirring at −78° C. for 1.5 h, the solution of the lithiated benzothiazole was transferred via a needle into an ice-cold suspension of 5-chloroisatin (3.63 g, 20 mmol) in THF (70 ml). The reaction mixture was stirred at 0° C. for 1 h and then saturated ammonium chloride solution was added. The mixture was extracted three times with ethyl acetate and the combined organic layers were washed with saturated brine. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure, during which the intermediate starts to crystallize. Filtration and drying yielded 4.47 g of the intermediate as yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902379B2
Source datasetuspto-grants-2011_03
ORD IDord-d5b4259c52af42ddaf18e69ac2ea94c4
Source noteuspto-grants-2011_03