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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383876Generated: October 31, 2026

HCID 21188455, compound → HCID 15452531, compound

https://huagongshe.com/reaction/1383876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21188455HCID 21188455—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
ProductHCID 15452531HCID 1545253171.8%

Reaction Steps

N-carbomethoxy-5-(2-chloro-5-pyridyl)-7-aza-bicyclo[2.2.1]hept-2-ene 25 (16 mg) was dissolved in 3 ml methanol containing 7 mg 10% palladium on carbon. The mixture was hydrogenated under a slightly elevated pressure of hydrogen for one hour. After removal of catalyst and solvent, the residue was partitioned between ether and aqueous sodium bicarbonate. The aqueous layer was extracted with ether and the combined organic layer was dried over magnesium sulfate. Removal of solvent gave 10 mg of 7-carbomethoxy-2-(3-pyridyl)-7-azanorbornane (12). MS (CI) m/z 233 (M+1), H1-NMR 3.72, 3.66 (2s, N-COOCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255490B1
Source datasetuspto-grants-2001_07
ORD IDord-54354e7ac05f41ba83378d37e2d7cf18
Source noteuspto-grants-2001_07