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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060798Generated: October 31, 2026

Ethanol → HCID 57504924, compound

https://huagongshe.com/reaction/2060798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCesium carbonateHCID 10796—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
ReactantHCID 57504923HCID 57504923—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57504924HCID 5750492479%

Reaction Conditions

Temperature97 °C

Reaction Steps

A solution of N-((4aR,6R,7aS)-7a-(3-bromo-4-fluorophenyl)-6-hydroxy-4,4a,5,6,7,7a-hexahydrocyclopenta[d][1,3]thiazin-2-yl)benzamide (0.588 g, 1.31 mmol) in a mixture of 1,2-dimethoxyethane (8 mL), ethanol (4 mL) and water (4 mL) is purged with nitrogen and is heated to 97° C. Pyrimidine-5-boronic acid (0.810 g, 6.54 mmol), cesium carbonate (2.56 g, 7.84 mmol) and bis(triphenylphosphine)palladium(II) chloride (0.184 g, 0.261 mmol) is added in a single portion and the reaction is heated at 97° C. for 30 minutes. The reaction is cooled, diluted with water and is extracted twice with ethyl acetate. The organic layer is dried over sodium sulfate and the crude product is purified by silica gel chromatography with a linear gradient of 0% to 40% ethyl acetate in dichloromethane over 20 minutes to give the title compound (0.464 g, 79%). ES/MS m/e: 449 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278441B2
Source datasetuspto-grants-2012_10
ORD IDord-1caba26cc8e3473b83bd0dfb1a2fbc39
Source noteuspto-grants-2012_10