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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871435Generated: October 30, 2026

3-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline → HCID 58267770, compound

https://huagongshe.com/reaction/871435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(6,7-Dimethoxy-4-quinazolinyl)oxy]anilineHCID 49841002—
ReactantHCID 66876449HCID 66876449—
ProductHCID 58267770HCID 5826777046.7%

Reaction Steps

3-(6,7-dimethoxyquinazolin-4-yloxy)aniline from Example 113A (89 g, 0.3 mmol) and phenyl 3-methoxy-5-(trifluoromethyl)phenylcarbamate from Example 115A (140 mg, 0.45 mmol) were reacted using the procedure in Example 115C to give 1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(3-methoxy-5-(trifluoromethyl)phenyl)urea (71 mg, 0.14 mmol, 46%). 1H NMR (300 MHz, DMSO-d6) δ 9.19 (s, 1H), 9.08 (s, 1H), 8.56 (s, 1H), 7.62-7.55 (m, 2H), 7.48 (s, 1H), 7.45-7.37 (m, 2H), 7.31-7.24 (m, 2H), 6.95 (d, 1H), 6.84 (s, 1H), 4.00 (s, 3H), 3.99 (s, 3H), 3.80 (s, 3H); LC-MS (ESI) m/z 515 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-aecdc921ef314897ad7f4ca791f1fabe
Source noteuspto-grants-2015_03