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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791213Generated: October 30, 2026

2-Amino-5-(trifluoromethyl)pyridine → (7-Bromo-quinazolin-4-yl)-(5-trifluoromethyl-pyridin-2-yl)-amine

https://huagongshe.com/reaction/1791213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant7-Bromo-4-chloroquinazolineHCID 16780855—
Product(7-Bromo-quinazolin-4-yl)-(5-trifluoromethyl-pyridin-2-yl)-amineHCID 11485491—

Reaction Steps

Heat a mixture of 7-bromo-4-chloro-quinazoline (200 mg, 0.821 mmol) and 2-amino-5-trifluoromethyl-pyridine (239 mg, 1.48 mmol) at 230° C. for 2 minutes. Cool and partition the solid residue between EtOAc and 10% NaOH. Dry the EtOAc layer (Na2SO4), remove the solvent under reduced pressure, and purify via flash chromatography to yield (7-bromo-quinazolin-4-yl)-(5-trifluoromethyl-pyridin-2-yl)-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074799B2
Source datasetuspto-grants-2006_07
ORD IDord-21e4402921fa4633ac07f6e8ca557001
Source noteuspto-grants-2006_07