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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968634Generated: October 30, 2026

Benzenamine, 3-ethynyl- → N-(3-ethynylphenyl)-7-nitroquinazolin-4-amine

https://huagongshe.com/reaction/1968634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactant4-Chloro-7-nitroquinazolineHCID 830680—
SolventIsopropanolHCID 3776—
ProductN-(3-ethynylphenyl)-7-nitroquinazolin-4-amineHCID 1604551994%

Reaction Steps

A mixture of 4-chloro-7-nitroquinazoline (2.0 g, 9.54 mmol), isopropanol (30 mL), and 3-ethynylbenzenamine (1.2 g, 10.00 mmol) was refluxed for 5 h. The reaction mixture was cooled to room temperature and refrigerated. The solid was filtered, washed with cold isopropanol several times, and dried in vacuo to give 2.6 g (94%) of N-(3-ethynylphenyl)-7-nitroquinazolin-4-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426430B2
Source datasetuspto-grants-2013_04
ORD IDord-a5b0009a281841efb168911fedbead1b
Source noteuspto-grants-2013_04