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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990702Generated: October 30, 2026

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

https://huagongshe.com/reaction/990702

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. over night. 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 MHz, DMSO) δ 4.59-4.63 (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 numberUS06462044B2
Source datasetuspto-grants-2002_10
ORD IDord-0ca1928c37e7487ba0c45d713a46dd8b
Source noteuspto-grants-2002_10