HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929025Generated: October 30, 2026
Potassium trimethylsilanolate → HCID 71667974, compound
https://huagongshe.com/reaction/929025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | HCID 89705347 | HCID 89705347 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71667974 | HCID 71667974 | 65.7% |
Reaction Steps
To a solution of 7-(cyclopropylsulfonyl)-4-fluoro-5-(2-fluoro-4-iodophenyl)-5H-imidazo[4′,5′:4,5]benzo[1,2-d]thiazol-6(7H)-one (50 mg, 0.09 mmol) in THF (5 mL) was added potassium trimethylsilanolate (19 mg, 0.14 mmol). After stirring at room temperature for 1 h, the reaction was quenched with saturated NH4Cl (aq., 5 mL). 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 as a white solid (30 mg, 63.1% yield). 1H NMR (400 MHz, CDCl3): δ 8.65 (s, 1H), 8.02 (s, 1H), 7.91 (d, 1H), 7.86 (s, 1H), 7.76 (d, 1H), 7.45 (m, 1H), 5.52 (s, 1H), 2.85 (m, 1H), 1.29 (m, 2H), 1.20 (m, 2H). MS APCI (+) m/z: 508.5 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290468B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-5a6c5e7c635d42629cff877d0aa45d92 |
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| Source note | uspto-grants-2016_03 |
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