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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176579Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 68497781, compound

https://huagongshe.com/reaction/1176579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-BromothiazoleHCID 76430—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 68497806HCID 68497806—
CatalystPalladium(II) trifluoroacetateHCID 2733347—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68497781HCID 68497781—

Reaction Steps

A baked-out Schlenk flask is initially charged under argon with 0.071 g of tri-tert-butylphosphine and 0.114 g of palladium trifluoroacetate. 1.3 ml of degassed toluene are added and the suspension is stirred under argon over 10 minutes. 0.700 g of benzyl 4-[4-(azetidin-3-yloxy)phenyl]-3-[4-(3-methoxypropyl)-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]piperidine-1-carboxylate (Example 257c), 0.265 g of tribasic potassium phosphate and 0.290 ml of bromothiazole are added and the reaction mixture is stirred at 80-85° C. over 16 hours. The reaction mixture is cooled, diluted with 20 ml each of brine and water and subsequently extracted with 40 ml of ethyl acetate. The organic phase is dried with sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a yellow resin from the residue by means of flash chromatography (SiO2 60F). Rf=0.15 (4:1 EtOAc-heptane); Rt=4.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-f4d4674a63c34ffb9ac094271ebd5eef
Source noteuspto-grants-2010_11