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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79035Generated: October 27, 2026

Lithium Hexamethyldisilazide → 7-((2-Fluoro-4-(methylthio)phenyl)amino)benzo[d]isothiazole-6-carboxylic acid

https://huagongshe.com/reaction/79035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Fluoro-4-(methylsulfanyl)anilineHCID 22025617—
Reactant7-Fluoro-benzo[d]isothiazole-6-carboxylic acidHCID 58374374—
SolventTetrahydrofuranHCID 8028—
Product7-((2-Fluoro-4-(methylthio)phenyl)amino)benzo[d]isothiazole-6-carboxylic acidHCID 6708357030%

Reaction Steps

To a solution of 2-fluoro-4-methylsulfanyl-phenylamine (628 mg, 4.0 mmol) in anhydrous THF (15 mL) at −78° C. was added a 1.0M solution of LHMDS in hexanes (6.0 mL, 6.0 mmol) under a nitrogen atmosphere. The reaction mixture was stirred for 5 minutes and a suspension of 7-fluoro-benzo[d]isothiazole-6-carboxylic acid (394 mg, 2.0 mmol) in anhydrous THF (15 mL) was added dropwise. The resultant mixture was stirred at −78° C. for 30 minutes, then allowed to reach room temperature and stirred for 18 hours before being quenched by addition of a 1M aqueous HCl (ca. 50 mL) and extracted with ethyl acetate. The organic layer was separated and washed with water followed by brine, dried (Na2SO4), filtered and evaporated in vacuo. The resultant residue was subjected to flash chromatography (Si—PPC, gradient 0% to 10%, MeOH in DCM) to give the title compound as a brown solid (200 mg, 30%). LCMS (method B): RT=3.67 min, [M+H]+=335

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-e2318b5052d94542818ab0fc37e85e57
Source noteuspto-grants-2014_09