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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzo-1,3-dioxole-5-methylamine | HCID 75799 | — |
| Reactant | 2,4,6-Trichloroquinazoline | HCID 10421510 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-((1,3-Benzodioxol-5-ylmethyl)amino)-2,6-dichloro quinazoline | HCID 22339865 | 96.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472425B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3f0a2d225fd54ab691031df5889ac26f |
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| Source note | uspto-grants-2002_10 |
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