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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367176Generated: October 28, 2026

N-Methylcyclohexylamine → HCID 23287725, compound

https://huagongshe.com/reaction/367176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantAmmonium thiocyanateHCID 15666—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Chloronicotinic acidHCID 76258—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 23287725HCID 2328772546.8%

Reaction Steps

The reaction procedure of Example 57 was followed except that 1.749 g (11.10 mmol) of 2-chloronicotinic acid, 15 ml of thionyl chloride, two droplets of DMF, 888 mg of ammonium thiocyanate, 15 ml of acetone, 1.32 g of N-methylcyclohexylamine and 10 ml of acetone were used. The resulting crude product was then recrystallized from ethanol to obtain 1.43 g of 2-(N-cyclohexyl-N-methylamino)-4H-pyrido[3,2-e]-1,3-thiazin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133258
Source datasetuspto-grants-2000_10
ORD IDord-636bb9cb69a7460c9933ea9c0004648a
Source noteuspto-grants-2000_10