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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822823Generated: November 2, 2026

Sodium Methoxide → 5-[[2-[N-(6-Bromopyridin-2-yl)amino]thiazol-5-yl]thio]-2-methylbenzoic acid

https://huagongshe.com/reaction/1822823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5-Mercapto-2-methyl-benzoic acidHCID 15404466—
Reactant6-Bromo-n-(5-bromo-2-thiazolyl)pyridin-2-amineHCID 22170424—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-[[2-[N-(6-Bromopyridin-2-yl)amino]thiazol-5-yl]thio]-2-methylbenzoic acidHCID 2217038481.3%

Reaction Conditions

Temperature54 °C

Reaction Steps

A suspension of 2-[(6-bromo-2-pyridinyl)amino]-5-bromothiazole (100 mg, 0.3 mmol), 3-carboxy-4-methylthiophenol (170 mg, 0.98 mmol) and sodium methoxide (210 μL, 25% w/w solution in methanol, 0.9 mmol) in methanol (4.9 mL) and THF (2 mL) was heated to 54° C. for 5.5 h. Supplemental sodium methoxide solution (1.42 mL) was added in portions over a period of 5 h. The mixture was heated to 54° C. for 16 h and concentrated. The residue was diluted with 1 N aqueous HCl solution at 0° C. and stirred for several minutes. The precipitated solid was filtered, washed several times with water and ether, and dried in vacuo over P2O5. Trituration with ether afforded the titled compound (103 mg, 81%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037926B2
Source datasetuspto-grants-2006_05
ORD IDord-4919c2a4e5a04252ac2ddc5bacb192be
Source noteuspto-grants-2006_05