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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214459Generated: October 31, 2026

Potassium Carbonate → HCID 12073477, compound

https://huagongshe.com/reaction/2214459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
ReactantHCID 21948051HCID 21948051—
SolventDimethylformamideHCID 6228—
ProductHCID 12073477HCID 12073477—

Reaction Steps

A solution of 0.3 g (1.04 mmol) of 7-fluoro-N,N,5-trimethyl-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]-indole-1-carboxamide (obtained in stage 3.2.), of 0.120 g (0.63 mmol) of cuprous iodide, of 0.20 g (1.45 mmol) of potassium carbonate and of 0.60 g (3.19 mmol) of 3-bromo-6-methoxypyridine in 50 ml of N,N-dimethylformamide is heated at 150° C. for 20 h. The reaction mixture is cooled and concentrated under reduced pressure. Dichloromethane, water and a sodium hydroxide solution (1M) are added. The organic phase is separated by settling, washed with water, dried over sodium sulphate, filtered and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica gel (eluent: dichloromethane/ethyl acetate: 100/0 to 0/100; then ethyl acetate/methanol: 95/5). The white solid obtained is recrystallized from a dichloromethane/ethyl acetate mixture and washed with diethyl ether. A white solid (0.26 g; 0.66 mmol) is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109194B2
Source datasetuspto-grants-2006_09
ORD IDord-1ec58ae872db4fa0ba2f1d74a2ed7085
Source noteuspto-grants-2006_09