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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444472Generated: October 29, 2026

p-Chlorothiophenol → 5-[(4-Chlorophenyl)sulfanyl]pyridin-2-amine

https://huagongshe.com/reaction/444472

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantSodium MethoxideHCID 10942334—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
Product5-[(4-Chlorophenyl)sulfanyl]pyridin-2-amineHCID 12912743—

Reaction Steps

2-Amino-5-bromopyridine (7.8 grams), 4-chlorothiophenol (9.2 grams), sodium methoxide (3.5 grams), and copper powder (1.0 gram) were reacted in 100 ml. of methanol, for 12 hours, in a bomb, in accordance with the procedures of J. Med. Chem. 21, 235 (1978). The reaction mixture was filtered, washed with methanol, and methanol removed by evaporation. The methanol washes were combined with ethyl acetate extracts of solids made after refluxing on a steam bath for one hour. Solvents were removed and the solids dissolved in ethyl acetate and filtered to remove insolubles. The liquid was passed over a silica column with ethyl acetate, and the fraction corresponding to the product amine (Rf ≅0.2) collected., yield 6.5 grams, m.p., 161°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264605
Source datasetuspto-grants-1981_04
ORD IDord-5b40d5c1b2344b7d891aefd799c3405e
Source noteuspto-grants-1981_04