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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442640Generated: October 30, 2026

1,3-Benzodioxole-5-carboxylic acid → 1,3-Benzodioxol-5-yl(3,6-dihydro-1(2H)-pyridinyl)methanone

https://huagongshe.com/reaction/442640

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—
Product1,3-Benzodioxol-5-yl(3,6-dihydro-1(2H)-pyridinyl)methanoneHCID 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 numberUS05891876
Source datasetuspto-grants-1999_04
ORD IDord-24fb296721a34359970fcd166d91a405
Source noteuspto-grants-1999_04