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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986253Generated: October 31, 2026

Oxalyl chloride → HCID 20158336, compound

https://huagongshe.com/reaction/986253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant9(10H)-Acridinone, 10-(2-(diethylamino)ethyl)-HCID 148883—
SolventDichloromethaneHCID 6344—
ProductHCID 20158336HCID 20158336—

Reaction Steps

A solution of 11.5 g of 10-[2-(diethylamino)ethyl]-9-acridanone in 250 ml of dichloromethane is treated at -5° and within 0.5 hour with 6.7 ml of oxalyl chloride, stirred at room temperature for 1 hour, the yellow crystals (9-chloro-10-[2-(diethylamino)ethyl]acridinium chloride) which have formed are filtered and washed successively with methylene chloride and petroleum ether. The material obtained is taken up in 200 ml of methanol, treated with 3.6 g of thiosemicarbazide and stirred at room temperature for about 18 hours. The precipitated salt is filtered and washed successively with ethanol and ether. There is obtained 10-[2-(diethylamino)ethyl]-9-acridanone thiosemicarbazone dihydrochloride (crystallizing with 1 mol of methanol) of melting point 124° (decomposition). This material is treated with 1N sodium hydroxide solution and extracted with dichloromethane. The solution is washed with water, dried and evaporated, whereupon the product is crystallized from acetonitrile. There is obtained 10-[2-(diethylamino)ethyl]-9-acridanone thiosemicarbazone of melting point 154°-156°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04711889
Source datasetuspto-grants-1987_12
ORD IDord-4fd62ed375404f83ae9f15a08ba58a95
Source noteuspto-grants-1987_12