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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479990Generated: October 28, 2026

Triethylamine → (R)-4-(6-Chloro-4,5-dimethyl-pyridazin-3-yl)-2-methyl-3,4,5,6-tetrahydro-2H [1,2']bipyrazinyl-5'-carboxylic acid methyl ester

https://huagongshe.com/reaction/1479990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 5-chloropyrazine-2-carboxylateHCID 406081—
Reactant3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazineHCID 59191518—
Solvent1,4-DioxaneHCID 31275—
Product(R)-4-(6-Chloro-4,5-dimethyl-pyridazin-3-yl)-2-methyl-3,4,5,6-tetrahydro-2H [1,2']bipyrazinyl-5'-carboxylic acid methyl esterHCID 5919162671%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (1.20 g, 4.88 mmol), 5-chloro-pyrazine-2-carboxylic acid methyl ester (946 mg, 5.37 mmol), triethylamine (3.40 mL, 24.4 mmol), and 1,4-dioxane (10 mL) are combined in a 100 mL round-bottom flask fitted with a reflux condenser and heated to 80° C. for 24 h. The reaction is then allowed to cool to room temperature and stirred for 48 h. A beige solid precipitates during this time which is isolated by filtration, rinsing with H2O. The precipitate is dried in vacuo to afford the title compound (1.30 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409871B2
Source datasetuspto-grants-2016_08
ORD IDord-c20448a61bbe40cab23f5a6605a3c41b
Source noteuspto-grants-2016_08