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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270084Generated: October 31, 2026

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

https://huagongshe.com/reaction/2270084

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) δ4.59-4.63 (d, 2 H), 5.98 (s, 2 H), 6.86 (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 numberUS06331543B1
Source datasetuspto-grants-2001_12
ORD IDord-55922f367c5a48b1b9b954d8b1c277a4
Source noteuspto-grants-2001_12