HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929027Generated: October 30, 2026
Potassium trimethylsilanolate → HCID 89704807, compound
https://huagongshe.com/reaction/929027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | 7-((1-allylcyclopropyl)sulfonyl)-4-fluoro-5-(2-fluoro-4-iodophenyl)-5H-imidazo[4',5':4,5]benzo[1,2-d]thiazol-6(7H)-one | HCID 89705366 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89704807 | HCID 89704807 | 91.3% |
Reaction Steps
To a solution of 7-((1-allylcyclopropyl)sulfonyl)-4-fluoro-5-(2-fluoro-4-iodophenyl)-5H-imidazo[4′,5′:4,5]benzo[1,2-d]thiazol-6(7H)-one (60 mg, 0.11 mmol) in THF (5 mL) was added potassium trimethylsilanolate (14 mg, 0.11 mmol). The reaction was stirred at room temperature for 1 h and quenched with saturated NH4Cl (aq.). The aqueous layer was extracted with EA (10 mL×2). The combined organic phase was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate, 5:1-3:1, v/v) to give the desired product (50 mg, 91.3% yield). 1H NMR (400 MHz, CDCl3): δ 8.67 (s, 1H), 7.97 (s, 1H), 7.92 (d, 1H), 7.78 (d, 1H), 7.46 (m, 1H), 6.82 (s, 1H), 6.64 (s, 1H), 5.75-5.58 (m, 1H), 5.05 (m, 2H), 2.90-2.80 (m, 1H), 2.10-2.00 (m, 1H), 1.95-1.86 (m, 2H), 1.25-1.10 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09290468B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-d45705c16cda458688efd18e323eed15 |
|---|
| Source note | uspto-grants-2016_03 |
|---|