Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416552Generated: October 31, 2026

Lawesson's reagent → N-[4-chloro-3-[(4-morpholinylimino)methyl]phenyl]-2-methyl-3-furancarbothioamide

https://huagongshe.com/reaction/1416552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminaHCID 9989226—
ReactantN-[4-chloro-3-[(4-morpholinylimino)methyl]phenyl]-2-methyl-3-furancarboxamideHCID 67563349—
SolventTolueneHCID 1140—
ProductN-[4-chloro-3-[(4-morpholinylimino)methyl]phenyl]-2-methyl-3-furancarbothioamideHCID 300194347.8%

Reaction Conditions

Temperature85 °C

Reaction Steps

A reaction mixture of N-[4-chloro-3-[(4-morpholinylimino)methyl]phenyl]-2-methyl-3-furancarboxamide (1.0 g), sodium bicarbonate (2.5 g), Lawesson's reagent (1.2 g) in toluene (25 ml) was heated at 85° C. for 4 hours. After cooling, the reaction mixture was passed through a plug of aluminum oxide, followed by elution with ether. Evaporation of the eluant gave 0.5 g of N-[4-chloro-3-[(4-morpholinylimino)methyl]phenyl]-2-methyl-3-furancarbothioamide as a yellow solid, mp 142-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05914351
Source datasetuspto-grants-1999_06
ORD IDord-455cfd4650004561aa01a7e9062e227f
Source noteuspto-grants-1999_06