Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447113Generated: October 29, 2026

Triethylamine → 2-[(R)-4-(6-Chloro-4,5-dimethyl-pyridazin-3-yl)-2-methyl-piperazin-1-yl]-4-trifluoromethyl-pyrimidine-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/447113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylateHCID 3696469—
Reactant3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazineHCID 59191518—
SolventDichloromethaneHCID 6344—
Product2-[(R)-4-(6-Chloro-4,5-dimethyl-pyridazin-3-yl)-2-methyl-piperazin-1-yl]-4-trifluoromethyl-pyrimidine-5-carboxylic acid methyl esterHCID 59191473—

Reaction Steps

Triethylamine (2.0 mL, 14.4 mmol, 2.9 eq) is added to a solution of 2-chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid methyl ester (1.25 g, 5.0 mmol, 1 eq), 3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (1.20 g, 5.0 mmol, 1 eq) in dichloromethane (40 mL) and the resulting solution is stirred at rt for 2 h. The reaction mixture is diluted with dichloromethane (50 mL) and washed with water (25 mL), then brine (25 mL). The organic layer is separated, dried over sodium sulfate and concentrated under reduced pressure to a white residue. The desired compound is isolated by silica gel chromatography (10-75% EtOAc/heptane) as a white solid (1.83 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481542B2
Source datasetuspto-grants-2013_07
ORD IDord-77ab1dd6cc604a189831aaac85d95c45
Source noteuspto-grants-2013_07