HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928978Generated: October 31, 2026
Potassium trimethylsilanolate → HCID 71667663, compound
https://huagongshe.com/reaction/928978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | HCID 89705472 | HCID 89705472 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71667663 | HCID 71667663 | 35.1% |
Reaction Steps
To a solution of 7-(cyclopropylsulfonyl)-4-fluoro-5-(2-fluoro-4-iodo phenyl)-5H-imidazo[4′,5′:4,5]benzo[1,2-d]oxazol-6(7H)-one (30 mg, 0.06 mmol) in THF (3 mL) was added potassium trimethylsilanolate (12 mg, 0.09 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 (5 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 (10 mg, 35.1% yield). 1H NMR (400 MHz, CDCl3): δ 8.15 (s, 1H), 7.88 (s, 1H), 7.46 (dd, 1H), 7.33 (s, 1H), 7.23 (dd, 1H), 6.15 (m, 1H), 5.49 (s, 1H), 2.55 (m, 1H), 1.01 (m, 2H), 0.92 (m, 2H). MS APCI (+) m/z: 492.5, [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-356a7391fd9d4b5795feab458883a87d |
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| Source note | uspto-grants-2016_03 |
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