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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608202Generated: October 31, 2026

Ethanethiol → 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2-hydroxybenzamide

https://huagongshe.com/reaction/1608202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
Reactant4-amino-N-((4-benzyl-2-morpholinyl)methyl)-5-chloro-2-methoxybenzamideHCID 197237—
SolventDimethylformamideHCID 6228—
Product4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2-hydroxybenzamideHCID 1488197870.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred suspension of 60% sodium hydride (0.52 g) in dimethylformamide (20 ml) is added under ice-coolinga solution of ethanethiol (0.81 g) in dimethylformamide (5 ml). After the mixture is stirred at 25° C. for 0.5 hour, 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2-methoxybenzamide (3.4 g) is added, and the mixture is stirred at 100° C. for 1 hour. After cooling, the reaction mixture is evaporated under reduced pressure. The residue is diluted with water, washed with chloroform, and neutralized with 10% hydrochloric acid. The precipiate is collected, washed with water, and recrystallized from isopropyl alcohol to give the monohydrate of the title compound (2.3 g), mp 153°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870074
Source datasetuspto-grants-1989_09
ORD IDord-fcafa61a702442e7bdd3a3bf7b8ff2a4
Source noteuspto-grants-1989_09