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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436265Generated: November 1, 2026

1,3-Benzodioxol-5-amine → 4-Quinazolinamine, N-1,3-benzodioxol-5-yl-2-chloro-N-methyl-

https://huagongshe.com/reaction/1436265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzodioxol-5-amineHCID 84310—
Reactant2,4-DichloroquinazolineHCID 252886—
ReactantN-(2H-1,3-Benzodioxol-5-yl)-2-chloroquinazolin-4-amineHCID 22692858—
Product4-Quinazolinamine, N-1,3-benzodioxol-5-yl-2-chloro-N-methyl-HCID 11536924—

Reaction Steps

(2-Chloro-quinazolin-4-yl)-(3,4-methylenedioxyphenyl)-amine: The title compound was prepared from 3,4-methylenedioxyphenylamine and 2,4-dichloroquinazoline by a procedure similar to example 1b and was isolated as solids (45% yield). 1H NMR (CDCl3): 7.81-7.83 (m, 3H), 7.51-7.56 (m, 2H), 7.44 (d, 1H, J=2.1), 6.98 (dd, 1H, J=2.1, 8.1), 6.82 (d, 1H, J=8.1), 6.01 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618975B2
Source datasetuspto-grants-2009_11
ORD IDord-7967e917c3eb4544a26885d171b5a7e7
Source noteuspto-grants-2009_11