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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415693Generated: October 27, 2026

Hydrochloric Acid → 1-(Methylsulfanyl-pyrimidine-4-carbonyl)hexahydro-pyridazine-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/2415693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2-Methylsulfanyl-pyrimidine-4-carbonyl chlorideHCID 11542901—
ReactantMethyl hexahydropyridazine-3-carboxylateHCID 20596490—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfanyl-pyrimidine-4-carbonyl)hexahydro-pyridazine-3-carboxylic acid methyl esterHCID 2352687036%

Reaction Steps

To a solution of hexahydro-pyridazine-3-carboxylic acid methyl ester (1.5 g, 8.3 mmol) in CH2Cl2 (80 mL) is added 2-methylsulfanyl-pyrimidine-4-carbonyl chloride, 16, (1.41 g, 7.5 mmol) and triethylamine (1.2 mL, 8.3 mmol). The mixture is stirred at room temperature for 3 hours. The reaction solution is then diluted with1 N HCl (100 mL) and the organic phase is decanted. The aqueous phase is extracted with additional solvent and the organic layers are combined, dried, and concentrated in vacuo. The crude product is purified over silica(ethyl acetate/hexane 1:1) to afford 0.9 g (36% yield) of the desired product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821971B2
Source datasetuspto-grants-2004_11
ORD IDord-dc92d9e05a3844878c54af1fabfcebb6
Source noteuspto-grants-2004_11