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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2-Fluoro-4-(methylsulfanyl)aniline | HCID 22025617 | — |
| Reactant | 7-Fluoro-benzo[d]isothiazole-6-carboxylic acid | HCID 58374374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-((2-Fluoro-4-(methylthio)phenyl)amino)benzo[d]isothiazole-6-carboxylic acid | HCID 67083570 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841462B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e2318b5052d94542818ab0fc37e85e57 |
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| Source note | uspto-grants-2014_09 |
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