Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 70248079 | HCID 70248079 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21717497 | HCID 21717497 | 181.8% |
Reaction Steps
In 20 ml of ethanol was dissolved 1.01 g (3.00 mmol) of (t-butyl) 5-t-butoxycarbonyl-4,5,6,7-tetrahydropyrazolo[4,5-c]pyridin-1-acetate, and under ice-cooling, 0.39 g (3.30 mmol) of thionyl chloride was added to the solution and the resulting mixture was stirred at 80° C. for 3 hours. The reaction mixture was concentrated under reduced pressure, the residue was washed with ethyl acetate and dried to obtain 0.90 g (3.00 mmol) of the title compound as pale yellowish powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265418B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-08e4c1c3657541929dd9f642726b8b03 |
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| Source note | uspto-grants-2001_07 |
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