HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225448Generated: October 30, 2026
Potassium Hydroxide → HCID 57753033, compound
https://huagongshe.com/reaction/225448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 11178857 | HCID 11178857 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57753033 | HCID 57753033 | — |
Reaction Steps
A mixture of {1-[7-(4-bromo-2,6-dimethyl-phenyl)-2,6-dimethyl-thieno[3,2-d]pyrimidin-4-yl]-piperidin-4-yl}-acetonitrile (350 mg) and KOH (492 mg) in a mixture of EtOH (1.5 mL) and H2O (1.0 mL) in a sealed tube was heated at 105° C. for 3 hours. After concentration of the reaction mixture under reduced pressure, 5% KHSO4 aqueous solution was added and extracted with CHCl3. The organic layer washed with brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by a silica gel column chromatography (silica gel: Wako Gel (C200), eluent: CHCl3/methanol=20:1) to obtain the title compound (164 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557111B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-3b2763fd6cd142e1b172eb5fc93aa1a4 |
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| Source note | uspto-grants-2009_07 |
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