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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235845Generated: October 30, 2026

1,3-Benzodioxole-5-carboxylic acid → HCID 13579410, compound

https://huagongshe.com/reaction/235845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzodioxole-5-carboxylic acidHCID 7196—
Reactant7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
ProductHCID 13579410HCID 1357941039.3%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is similar to that described in Example 1, but starting with 3,4-methylenedioxybenzoic acid (16.6 g), N,N'-carbonyldiimidazole (16.2 g) and 2-amino-7-chloro-1,8-naphthyridine (11.7 g). The product produced by precipitation in water (15.7 g; m.p. 256° C.) is dissolved in 1-propanol (1000 cc). After 16 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with 1-propanol (3×20 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-chloro-1,8-naphthyridin-2-yl)-3,4-methylenedioxybenzamide (8.4 g) is produced, m.p. 256° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642308
Source datasetuspto-grants-1987_02
ORD IDord-6d2d2db60a1e4a6290f437f66107e198
Source noteuspto-grants-1987_02