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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTert-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}carbamateHCID 69371253—
Reactant6-Iodo-[1,2,4]triazolo[4,3-a]pyridineHCID 69371559—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product(3S)-1-[(2S,3S)-2-Amino-3-[4-([1,2,4]triazolo[4,3-alpha]pyridin-6-yl)phenyl]-1-oxobutanyl]-3-fluoropyrrolidineHCID 10451602—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157490B2
Source datasetuspto-grants-2007_01
ORD IDord-cd374eb264394065945a5ca975db0abd
Source noteuspto-grants-2007_01