Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871478Generated: October 31, 2026

3-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline → HCID 56953738, compound

https://huagongshe.com/reaction/871478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(6,7-Dimethoxy-4-quinazolinyl)oxy]anilineHCID 49841002—
ReactantHCID 59394199HCID 59394199—
ProductHCID 56953738HCID 5695373859%

Reaction Steps

The title compound was prepared as described in Example 113C using 3-(6,7-dimethoxyquinazolin-4-yloxy)aniline from Example 113A (90 mg, 0.3 mmol) and phenyl 5-isopropylisoxazol-3-ylcarbamate from the previous step (110 mg, 0.45 mmol) to give 1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-isopropylisoxazol-3-yl)urea (79 mg, 59%) as a white solid after purification by preparative HPLC (phenylhexyl reverse phase column). 1H NMR (300 MHz, DMSO-d6) δ 9.57 (s, 1H), 9.01 (s, 1H), 8.56 (s, 1H), 7.57 (s, 2H), 7.41 (t, 2H) 7.27 (d, 1H), 6.99 (d, 1H), 6.49 (s, 1H), 4.00 (s, 6H), 3.01-2.99 (m, 1H), 1.22 (d, 6H); LC-MS (ESI) m/z 450 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-8b95c63af6184df28646031e5590e009
Source noteuspto-grants-2015_03