Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850280Generated: October 30, 2026

Piperidine → HCID 58547146, compound

https://huagongshe.com/reaction/1850280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 3-(3-chloropyrazin-2-yl)azetidine-1-carboxylateHCID 59351411—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 58547146HCID 5854714675.99%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-(3-chloro-pyrazin-2-yl)-azetidine-1-carboxylic acid tert-butyl ester (7) (200 mg, 0.74 mmol, see Preparation 2) and piperidine (69.2 mg, 0.84 mmol) in DMSO (5 mL) was added Et3N (149.5 mg, 1.48 mmol). The reaction mixture was stirred at 100° C. overnight. The reaction mixture was diluted with water, extracted with EtOAc (30 mL×3). The combined organic extracts were washed with water (30 mL) and brine (30 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel to give tert-butyl 3-(3-(piperidin-1-yl)pyrazin-2-yl)azetidine-1-carboxylate (74). (194 mg, 0.56 mmol, yield 75.99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-3089dd40b428470e8a9e16cffa7287bb
Source noteuspto-grants-2015_02