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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988000Generated: November 2, 2026

Potassium Acetate → HCID 11047852, compound

https://huagongshe.com/reaction/988000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantHCID 10908472HCID 10908472—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
Solvent1-PentanolHCID 6276—
ProductHCID 11047852HCID 11047852—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of tert-butyl 3-[1-(6-benzyloxy-7-fluoro-2-iodo-3-quinolylmethyl)-2-oxo-1,2-dihydro-4-pyridinyl]-3-hydroxypentanoate (obtained according to 1.i, 1.6 g, 2.4 mmol), tetrabutylammonium bromide (0.77 g, 2.4 mmol), potassium acetate (0.24 ml, 2.4 mmol) and palladium acetate (0.55 g, 2.4 mmol) in anhydrous amyl alcohol (30 ml) is heated at 80° C. under an argon atmosphere for 3 hours, then concentrated under reduced pressure. The residue is taken up in methanol (50 ml) and dichloromethane (100 ml), filtered through celite then concentrated under reduced pressure in order to produce a pink solid which is taken up in methanol, then treated with hot activated carbon. The liquor obtained by filtration is concentrated to 5 ml, then placed at 4° C. for 16 hours. The resulting precipitate is collected by filtration and washed with diethyl ether in order to produce, after drying, 370 mg (29%) of a white solid, m.p. >275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632946B2
Source datasetuspto-grants-2003_10
ORD IDord-b320d05ef1694afaa0365d920c62570c
Source noteuspto-grants-2003_10