Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23138514 | HCID 23138514 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23138832 | HCID 23138832 | 87% |
Reaction Steps
To (E)-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-3-({1-[2-(ethoxycarbonyl)ethyl]-1H-1,2,3-triazol-5-yl}methylidene)-4-sulfanylpiperidine hydrochloride (500 mg) was added 3 N aqueous hydrochloric acid solution (20 ml) and the resulting mixture was stirred at 50° C. for 3 hours. After the reaction mixture was concentrated under reduced pressure, the residue was purified using preparative HPLC [YMC-Pack ODS-A; YMC, eluent: acetonitrile/0.024 N aqueous hydrochloric acid solution (25:75, v/v)] to afford the title compound (410 mg, yield: 87%) as a pale colourless amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829580B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b400d3e93b6e4939be2c6f5bc31175e9 |
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| Source note | uspto-grants-2010_11 |
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