Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351501Generated: November 1, 2026

2,3-Dichloropyridine → HCID 10291987, compound

https://huagongshe.com/reaction/1351501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropyridineHCID 16988—
Reactant4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
ProductHCID 10291987HCID 10291987—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of benzyl 4-(aminomethyl)piperidine-1-carboxylate (EXAMPLE 13, Step 1) (1 g, 4.03 mmol) and 2,3-dichloropyridine (0.25 g) was heated to 100° C. for 12 h. The reaction mixture was cooled and partitioned between EtOAc and pH5.2 citrate buffer. The organic layer was washed with brine, dried over anhydrous sodium sulfate and the solvent evaporated to give a crude product. Purification by flash column chromatography (5–50% EtOAc hexane) afforded the title compound. M.S (M+1): 360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217716B2
Source datasetuspto-grants-2007_05
ORD IDord-e7df6289f4a64e1885c5671ef4d8f31e
Source noteuspto-grants-2007_05