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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81697Generated: October 30, 2026

Potassium Carbonate → 2-{4-Amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamide

https://huagongshe.com/reaction/81697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-2-(chloromethyl)-4-methoxy-5-methylpyridine hydrochlorideHCID 66617932—
ReactantHCID 136403539HCID 136403539—
SolventDimethylformamideHCID 6228—
Product2-{4-Amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamideHCID 6661807484.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Dimethylformamide (1 ml) was added to 2-(4-amino-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl)-N-methylacetamide trifluoroacetate (28 mg), 3-chloro-2-(chloromethyl)-4-methoxy-5-methylpyridine hydrochloride (36 mg), and potassium carbonate (69 mg). The resulting mixture was stirred at 60° C. for 2.5 hours. Thereafter, the insoluble matter was removed by filtration, and the solvent was then distilled away in a nitrogen stream. The resulting residue was dissolved in dimethyl sulfoxide (1 ml), and it was then purified by preparatory reverse-phase HPLC. The solvent was distilled away under reduced pressure, so as to obtain the title compound (27.0 mg) as a solid (amorphous substance).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846703B2
Source datasetuspto-grants-2014_09
ORD IDord-f3eeb77163c44ed98820b86697c318e4
Source noteuspto-grants-2014_09