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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458522Generated: November 1, 2026

1,3-Benzodioxole-5-carboxylic acid → 1-(1,3-Benzodioxol-5-ylcarbonyl)-1,2,3,6-tetrahydro-pyridine

https://huagongshe.com/reaction/1458522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzodioxole-5-carboxylic acidHCID 7196—
Reactant1,2,3,6-TetrahydropyridineHCID 12750—
Reactant1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Product1-(1,3-Benzodioxol-5-ylcarbonyl)-1,2,3,6-tetrahydro-pyridineHCID 11776063—

Reaction Steps

The product amide is made by the method employed for the preparation of Invention Compound V, which uses carbonyl diimidazole in order to activate piperonylic acid, or piperonyloyl chloride (available from Aldrich) can be combined with 1,2,3,6-tetrahydropyridine either in a suitable anhydrous solvent or without solvent. In either case, the isolation of product is performed in the same manner as done for Invention Compound V to give Invention Compound III as a white solid. EIMS m/z=231 (parent, 149 (base), and 121. 1H NMR δ 2.21 (br s, 2), 3.4-4.3 (br m, 4), 5.87 (m, 2), 6.00 (s, 2), 6.83 (d, 1, J=7.84 Hz), and 6.92-6.96 (dd and d, 2). 13C NMR δ 101.3 (--OCH2O--) and 169.9 ppm (carbonyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852008
Source datasetuspto-grants-1998_12
ORD IDord-7831979740fd4f97a9d3508258c224f9
Source noteuspto-grants-1998_12