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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993259Generated: October 29, 2026

Benzo-1,3-dioxole-5-methylamine → 4-((1,3-Benzodioxol-5-ylmethyl)amino)-2,6-dichloro quinazoline

https://huagongshe.com/reaction/993259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo-1,3-dioxole-5-methylamineHCID 75799—
Reactant2,4,6-TrichloroquinazolineHCID 10421510—
SolventEthanolHCID 702—
Product4-((1,3-Benzodioxol-5-ylmethyl)amino)-2,6-dichloro quinazolineHCID 2233986596.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 2,4,6-trichloroquinazoline (0.186 g, 0.80 mmol) in ethanol (20 mL) was heated to 55° C. and piperonylamine (0.145 g, 0.96 mmol) was added. The resulting mixture was stirred at 55° C. overnight. Volatiles were evaporated and the residue was partitioned between methylene chloride and saturated solution of ammonium hydroxide. The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuo to yield 0.268 g (96 % yield) of the title compound as a white solid. 1H NMR (300 ÊMt, DMSO) δ4.59-4.63 (d, 2 H), 5.98 (s, 2 H), 6.86 (s, 2 H), 6.96 (s, 1 H), 7.62-7.66 (d, 1 H), 7.79-7.84 (d, 1 H), 8.46 (s, 1 H), 9.24-9.28 (t, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472425B1
Source datasetuspto-grants-2002_10
ORD IDord-3f0a2d225fd54ab691031df5889ac26f
Source noteuspto-grants-2002_10