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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801566Generated: November 1, 2026

Piperidine-1-carboxamidine → HCID 178451770, compound

https://huagongshe.com/reaction/1801566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidine-1-carboxamidineHCID 205051—
ReactantSodiumHCID 5360545—
Reactanttert-Butyl 4-(3-ethoxy-3-oxopropanoyl)piperidine-1-carboxylateHCID 6618868—
SolventEthanolHCID 702—
ProductHCID 178451770HCID 17845177045.2%

Reaction Steps

Sodium (1 mol) was dissolved in anhydrous ethanol (400 mL). To the obtained solution, Piperidine-1-carboxamidine (0.5 mol) was carefully added in portions. Then 4-(2-Ethoxycarbonyl-acetyl)-piperidine-1-carboxylic acid tert-butyl ester (0.5 mol) was added dropwise, and the mixture was stirred at reflux for 4-6 h (monitored by TLC), cooled to room temperature, concentrated, diluted with water (300 mL) and acidified with acetic acid to pH-4. The formed precipitate was collected by filtration, washed with water and dried to afford 4-(6-Hydroxy-2-piperidin-1-yl-pyrimidin-4-yl)-piperidine-1-carboxylic acid tert-butyl ester (82 g, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349833B2
Source datasetuspto-grants-2013_01
ORD IDord-434481db6300419b9ac296f585ad607f
Source noteuspto-grants-2013_01