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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520320Generated: November 3, 2026

2-Fluoroaniline → HCID 67298112, compound

https://huagongshe.com/reaction/1520320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantHCID 86677067HCID 86677067—
SolventIsopropanolHCID 3776—
ProductHCID 67298112HCID 6729811216.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 4-chloro-6-methoxy-2-(pyridin-3-yl)quinazoline (80 mg, 0.293 mmol, 1.0 eq.) and 2-fluoroaniline (65 mg, 0.58 mmol, 2 eq.) in i-PrOH (5 mL) was stirred at 85° C. for 18 h. After the reaction was completed, the mixture was filtered, and the filter cake was washed with H2O (10 ml) and diethyl ether (10 mL). After drying, the crude product was purified by PREP-HPLC (Condition C: Gradient: B=5%-50%, Target Peak: at 7.2 min) to give 16.5 mg of N-(2-fluorophenyl)-6-methoxy-2-(pyridin-3-yl)quinazolin-4-amine as a yellow solid, yield 16.4%. LCMS m/z=347.0 (M+1) (Method A) (retention time=1.31 min). 1H-NMR (400 MHz, DMSO-d6): δ 10.08 (s, 1H), 9.33 (s, 1H), 8.72 (d, J=4.4 Hz, 1H), 8.66 (d, J=8.0 Hz, 1H), 8.80 (d, J=1.2 Hz, 1H), 7.88 (d, J=9.2 Hz, 1H), 7.70-7.65 (m, 2H), 7.58 (dd, J=8.8, 1.2 Hz, 1H), 7.44-7.35 (m, 3H), 3.97 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073890B2
Source datasetuspto-grants-2015_07
ORD IDord-98a306d764094079be0aec9e42fc065b
Source noteuspto-grants-2015_07