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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650538Generated: October 29, 2026

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

https://huagongshe.com/reaction/650538

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 numberUS06274600B1
Source datasetuspto-grants-2001_08
ORD IDord-94e0639fa9cf42209623e196ce4858d2
Source noteuspto-grants-2001_08