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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470392Generated: October 25, 2026

Sodium Carbonate → HCID 67997358, compound

https://huagongshe.com/reaction/470392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-[(5-bromopyrimidin-4-yl)sulfanyl]acetateHCID 66318500—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthonitrileHCID 67997556—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67997358HCID 6799735853%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 2-(5-bromopyrimidin-4-ylthio)acetate (220 mg, 0.84 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthonitrile (237 mg, 0.85 mmol) palladium tetrakis triphenylphoshine (46 mg, 0.04 mmol) and aqueous sodium carbonate solution (2M, 1.5 mL, 3 mmol) in dioxane (3 mL) was heated to 100° C. for 5 hours. The reaction mixture was allowed to cool to room temperature and aqueous sodium hydroxide solution added (1M, 30 mL). The mixture was washed with ethyl acetate (2×20 mL), and the aqueous layer acidified to pH 4 resulting in formation of a precipitate which was isolated by filtration and dried under vacuum to yield 2-(5-(4-cyanonaphthalen-1-yl)pyrimidin-4-ylthio)acetic acid (143 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629278B2
Source datasetuspto-grants-2014_01
ORD IDord-d60a26cff6d84c62ae64d0427a7577b2
Source noteuspto-grants-2014_01