Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235269Generated: October 31, 2026

N-Methylformanilide → HCID 23353992, compound

https://huagongshe.com/reaction/235269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylformanilideHCID 66737—
ReactantHCID 10782547HCID 10782547—
SolventChlorine monoxideHCID 24646—
ProductHCID 23353992HCID 2335399246.1%

Reaction Steps

A mixture of 0.45 g of N-methylformanilide in 0.33 ml of phosphrus oxychloride was stirred at room temperature for an hour and 0.5 g of 2-(4 -chlorophenyl)-2,5,6,7-tetrahydro-3H-thieno-[2',3':6,7]cyclohepta[1,2-c]pyridazin-3-one was added thereto. After stirring at room temperature for 2 hours, the mixture was poured into ice-cold water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was chromatographed on a silica gel (SiO2 :40 g) column using chloroform as an eluent. The resulting solid was recrystallized from a mixed solvent of chloroform and ethanol to give 0.25 g of 2-(4-chlorophenyl)-9-formyl-2,5,6,7-tetrahydro-3H-thieno-[2',3':6,7]-cyclohepta[1,2-c]pyridazin-3-one as a pale yellow powder, melting at 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597918
Source datasetuspto-grants-1997_01
ORD IDord-ffef500251f94e9dae2e141c05282046
Source noteuspto-grants-1997_01