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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479969Generated: October 28, 2026

Ethyl 4-piperidinecarboxylate → 1-(6-Benzyl-4,5-dimethyl-pyridazin-3-yl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1479969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Benzyl-6-chloro-4,5-dimethylpyridazineHCID 59191487—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(6-Benzyl-4,5-dimethyl-pyridazin-3-yl)-piperidine-4-carboxylic acid ethyl esterHCID 6717682661.7%

Reaction Conditions

Temperature210 °C

Reaction Steps

To a solution of 3-benzyl-6-chloro-4,5-dimethyl-pyridazine (1.0 g, 4.31 mmol) in NMP (10 mL) is added piperidine-4-carboxylic acid ethyl ester (2.0 g, 12.9 mmol) and DIPEA (3.7 mL, 21.6 mmol). The mixture is heated in microwave at 210° C. for 1.5 h. The mixture is concentrated at 80° C. by rotovaporation. The crude product is purified by HPLC (CH3CN/H2O: 22%˜45% with 0.1% TFA) to give 1-(6-benzyl-4,5-dimethyl-pyridazin-3-yl)-piperidine-4-carboxylic acid ethyl ester (0.94 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409871B2
Source datasetuspto-grants-2016_08
ORD IDord-561067037bbd4d95a5ec858532eac144
Source noteuspto-grants-2016_08