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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399084Generated: October 30, 2026

HCID 21188455, compound → HCID 15452531, compound

https://huagongshe.com/reaction/399084

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 numberUS05817679
Source datasetuspto-grants-1998_10
ORD IDord-bac22529379045fb81d37336e7a5fff9
Source noteuspto-grants-1998_10