Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093060Generated: November 3, 2026

[(4-methoxyphenyl)amino]carbonitrile → HCID 178492303, compound

https://huagongshe.com/reaction/2093060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(4-methoxyphenyl)amino]carbonitrileHCID 10931588—
ReactantN-(2-aminophenyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamideHCID 58117006—
SolventChlorobenzeneHCID 7964—
ProductHCID 178492303HCID 178492303—

Reaction Steps

A solution of 4-methoxy-phenyl-cyanamide (2 eq) obtained in step I above and N-(2-aminophenyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamide obtained in step VIII of example I (1.0 eq) in chlorobenzene was refluxed for 6 h. Solvent was evaporated and the residue was treated with ethereal HCl at room temperature for 5-15 h. Solvent was evaporated and the residue was dissolved in methanol—DCM system and neutralized. Organic layer was separated, dried on anhydrous Na2SO4 and concentrated under reduced pressure to afford crude product, which was then purified, by either column chromatography or preparative HPLC to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440830B2
Source datasetuspto-grants-2013_05
ORD IDord-599c697f744a4866bc7cfc6c3ee056ac
Source noteuspto-grants-2013_05