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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995847Generated: October 30, 2026

Ethanethiol → 5-[(4-Chlorophenyl)methoxy]pyridine-2-carboxamide

https://huagongshe.com/reaction/1995847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodiumHCID 5360545—
Reactant5-Methoxypyridine-2-carboxamideHCID 20486069—
ReactantHCID 131713102HCID 131713102—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-[(4-Chlorophenyl)methoxy]pyridine-2-carboxamideHCID 20486110—

Reaction Steps

To 5-methoxy-2-pyridylcarboxamide (2 g, 13.2 mmol) in 5 ml of DMF at RT is added the sodium salt of ethanethiol (26.3 mmol) in DMF (61.5 ml). The slurry is heated to 110° with stirring for about 15 minutes. The reaction is cooled to 50° and 40 ml of DMF is added. After 0.5 hour, the reaction is cooled to 10° & 4-chlorobenzyl chloride (2.47 g, 15.4 mmol) is added. The reaction is allowed to warm to RT and is stirred for 3 days. About 0.5 ml of 4-chlorobenzyl chloride/DMF (0.21 g/l ml) is added. After 2 hours at RT, the reaction is poured into ice water and ethyl acetate. The ethyl acetate is separated off, and the water layer is extracted with ethyl acetate (4X). The combined organic layers are washed with water and with brine, dried, filtered and rotoevaporated. The residue is washed with 20% ether/hexane (4X). The liquid is pipetted off and the residue is rotoevaporated to give 5-(4-chlorobenzyloxy)-2-pyridylcarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04406689
Source datasetuspto-grants-1983_09
ORD IDord-7bfc2f45b81b4f31946a22ba3dcb72ae
Source noteuspto-grants-1983_09