HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374637Generated: October 30, 2026
p-Toluenesulfonic acid → Denagliptin Tosylate
https://huagongshe.com/reaction/2374637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | tert-Butyl ((1S)-1-[bis(4-fluorophenyl)methyl]-2-[(2S,4S)-2-cyano-4-fluoro-1-pyrrolidinyl]-2-oxoethyl)carbamate | HCID 68536750 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Denagliptin Tosylate | HCID 11466916 | 70% |
Reaction Steps
A 10L reactor equipped with overhead stirring was charged with a slurry of tert-Butyl {(1S)-1-[bis(4-fluorophenyl)methyl]-2-[(2S,4S)-2-cyano-4-fluoro-1-pyrrolidinyl]-2-oxoethyl}carbamate (500 g, 1 wt, 1 eq) in ethanol (3.5L, 7 vol). To this solution was added para-toluenesulfonic acid (403g, 0.806 wt, 2 eq). This solution was heated to 60° C., and was allowed to stir at this temperature for 12 hours. The reaction mixture was cooled to 5° C. and was stirred at this temperature for 30 minutes. The solids were collected by filtration, washed with ethanol (2×1 L), and dried to constant weight in a 50° C. vacuum oven. Yield: 70-80% over 2 steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462641B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-10e53fb25412461bb53daaf1303a7be5 |
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| Source note | uspto-grants-2008_12 |
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