Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86609418 | HCID 86609418 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86609421 | HCID 86609421 | 42% |
Reaction Steps
To a solution of (E)-4-(acetylsulfanyl)-3-{[1-(carboxymethyl)-1H-pyrazol-3-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]piperidine hydrochloride (190 mg) in dichloromethane (15 ml) were added isobutyl chloroformate (0.06 ml) and triethylamine (0.18 ml) under ice-cooling, and the resulting mixture was stirred at the same temperature for 30 minutes. To this reaction mixture was added 28% aqueous ammonia solution (0.03 ml), and the resulting mixture was stirred at room temperature for 45 minutes. After stirring, saturated aqueous sodium hydrogencarbonate solution was added to the reaction mixture and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of methanol and dichloromethane (1:19) as the eluent to afford the title compound (80 mg, yield: 42%) as a yellow oil.
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-698c3f924c17434b8b7d535ad0ada377 |
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| Source note | uspto-grants-2010_11 |
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