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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929075Generated: October 30, 2026

Potassium trimethylsilanolate → HCID 71666209, compound

https://huagongshe.com/reaction/929075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium trimethylsilanolateHCID 23668039—
ReactantHCID 89705395HCID 89705395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71666209HCID 7166620952.7%

Reaction Steps

To a solution of 7-(cyclopropylsulfonyl)-4-fluoro-5-(2-chloro-4-bromophenyl)-5H-imidazo[4′,5′:4,5]benzo[1,2-d][1,2,3]thiadiazol-6(7H)-one (60 mg, 0.12 mmol) in THF (5 mL) was added potassium trimethylsilanolate (16 mg, 0.12 mmol). After stirring at room temperature for 1 h, the reaction was quenched with saturated NH4Cl (aq.). The aqueous layer was extracted with ethyl acetate (10 mL×2). The combined organic phase was washed with brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residual crude product was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate, 5:1-3:1, v/v) to give the corresponding product (30 mg, 52.7% yield). 1H NMR (400 MHz, CDCl3): δ 8.25 (s, 1H), 8.02-7.98 (m, 1H), 7.85 (m, 1H), 7.60-7.56 (m, 1H), 7.14 (s, 1H), 6.83 (s, 1H), 2.81-2.72 (m, 1H), 1.33 (m, 2H), 1.15 (m, 2H). MS APCI (+) m/z: 478.8, [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290468B2
Source datasetuspto-grants-2016_03
ORD IDord-7a2f47996dfd401ab2b92f58bc9601c3
Source noteuspto-grants-2016_03