HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372467Generated: October 28, 2026
Potassium Phosphate, Tribasic → (3S)-1-[(2S,3S)-2-Amino-3-[4-([1,2,4]triazolo[4,3-alpha]pyridin-6-yl)phenyl]-1-oxobutanyl]-3-fluoropyrrolidine
https://huagongshe.com/reaction/1372467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tert-butyl{(1s,2s)-1-{[(3s)-3-fluoropyrrolidin-1-yl]carbonyl}-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propyl}carbamate | HCID 69371253 | — |
| Reactant | 6-Iodo-[1,2,4]triazolo[4,3-a]pyridine | HCID 69371559 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3S)-1-[(2S,3S)-2-Amino-3-[4-([1,2,4]triazolo[4,3-alpha]pyridin-6-yl)phenyl]-1-oxobutanyl]-3-fluoropyrrolidine | HCID 10451602 | — |
Reaction Steps
To a stirred solution of the product (48.0 mg, 0.195 mmol) from Step B in 0.75 mL of ethylene glycol dimethyl ether and 0.75 mL of water was added 62.0 mg (0.13 mmol) of (3S)-1-[(2S,3S)-2-[(tert-butoxycarbonyl)amino]-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1-oxobutanyl]-3-fluoropyrrolidine from Example 10, Step B, 1,1′-bis(diphenylphosphino)ferrocene palladium(II) chloride (21.0 mg, 0.26 mmol) and potassium phosphate (83 mg, 0.39 mmol). The reaction mixture was heated at 90° C. for 16 h, and then allowed to cool to room temperature. The mixture was diluted with ethyl acetate, and the solution was washed sequentially with water and saturated aqueous brine, dried (magnesium sulfate), and concentrated under reduced pressure in vacuo to yield the crude coupled product, which was purified by preparative thin layer chromatography (silica gel, 5% methanol/dichloromethane eluant). The resultant product was dissolved in 1 mL of dichloromethane and was treated with 1 mL of trifluoroacetic acid. The reaction was stirred at room temperature for 1 h, and was then concentrated under reduced pressure. The residue was purified by preparative thin layer chromatography (silica gel, 10% methanol/1% ammonium hydroxide/dichloromethane eluant) to afford the title compound. LC/MS 368.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157490B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-cd374eb264394065945a5ca975db0abd |
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| Source note | uspto-grants-2007_01 |
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