HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842023Generated: October 31, 2026
Potassium Hydroxide → HCID 22617853, compound
https://huagongshe.com/reaction/842023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 69967398 | HCID 69967398 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22617853 | HCID 22617853 | 78% |
Reaction Steps
To a stirred solution of {2-[3-(2,6-dichloro-4-trimethylsilanylethynyl-phenyl)-2,5-dimethyl-pyrazolo[1,5-a]pyrimidin-7-ylamino]-ethyl}-(tetrahydro-pyran-4-yl)-carbamic acid tert-butyl ester (1.2 g, 2.0 mmol) in ethanol (2 mL) was added KOH (0.2 g, 8 mmol). After 1 hour, the reaction was cooled to 0° C. and 1:1 ethanol/concentrated aqueous hydrochloric acid (4 mL) was added and the mixture was allowed to warm to room temperature. After 1 day, the reaction was concentrated under reduced pressure, extracted from saturated aqueous sodium bicarbonate with methylene chloride, the combined extracts were dried (Na2SO4), concentrated under reduced pressure, and then chromatographed (4:1 to 10:3 to 3:2 ethyl acetate/methanol) to afford the title compound (0.70 g, 78%) as an off-white solid: +APcI MS (M+1)+458; 1H NMR (methanol-d4) δ: 7.58 (d, 1H), 6.10 (s, 1H), 3.76 (s, 1H), 2.39 (s, 3H), 2.23 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372743B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-4ef7d816d0cf471d9e24e07398b7b1d9 |
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| Source note | uspto-grants-2002_04 |
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