Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Sitagliptin enamine | HCID 29986152 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Bis(norbornadiene)rhodium(I) tetrafluoroborate | HCID 10915722 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Sitagliptin | HCID 4369359 | — |
Reaction Steps
Into a flask were charged bis(norbornadiene)rhodium(I) tetrafluoroborate {[Rh(nbd)2]BF4}(41.55 mg, 0.1 mmol), Ligand D (69.73 mg, 0.1 mmol) and the enamine amide 2-4 (45 g, 111.1 mmol) under a nitrogen atmosphere. To this mixture a solvent mixture of 37.5 mL methanol (extra dry and degassed) and 112.5 mL 2,2,2-trifluoroethanol (distilled and degassed) were added. The slurry was then transferred under nitrogen into an stainless steel autoclave and sealed. The autoclave was then heated to 50° C. and pressurized to 500 psig with hydrogen. A sample taken after 17 hours was analyzed using HPLC, which confirmed the end of the reaction giving 94% assay yield and 94% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495123B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-cff681f700be4f089cd0a8a419ea1983 |
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| Source note | uspto-grants-2009_02 |
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