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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631386Generated: October 30, 2026

HCID 18004932, compound → HCID 56953871, compound

https://huagongshe.com/reaction/631386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18004932HCID 18004932—
Reactant3-[(6,7-Dimethoxy-4-quinazolinyl)oxy]anilineHCID 49841002—
ProductHCID 56953871HCID 5695387144%

Reaction Steps

The title compound was prepared according to the procedure described in Example 113C, by using compound 3-(6,7-dimethoxyquinazolin-4-yloxy)aniline from Example 113A (90 mg, 0.3 mmol) and compound phenyl 3-phenylisoxazol-5-ylcarbamate from the previous step (126 mg, 0.45 mmol) to afford 1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(3-phenylisoxazol-5-yl)urea as a white solid (63.34 mg, 44%). 1H NMR (300 MHz, DMSO-d6) δ 10.4 (s, 1H), 9.14 (s, 1H), 8.5 (s, 1H), 7.83 (d, 2H), 7.83-7.48 (m, 7H), 7.42 (d, 1H), 7.00 (d, 1H), 6.56 (s, 1H), 4.00 (s, 6H); LC-MS (ESI) m/z 484 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-3349fbd4950648ff9621b3c79c8fecec
Source noteuspto-grants-2016_04