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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917821Generated: October 30, 2026

3-(6-(Benzyloxy)-7-methoxyquinazolin-4-yloxy)aniline → 4-(3-Aminophenoxy)-7-methoxyquinazolin-6-ol

https://huagongshe.com/reaction/1917821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(6-(Benzyloxy)-7-methoxyquinazolin-4-yloxy)anilineHCID 66877522—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
Product4-(3-Aminophenoxy)-7-methoxyquinazolin-6-olHCID 6687610774.3%

Reaction Steps

A mixture of 3-(6-(benzyloxy)-7-methoxyquinazolin-4-yloxy)aniline (3.64 g, 0.00974 mol) and Pd/C (10%) in ethanol/THF (400 mL, 3/1) was hydrogenated at 1 atm. of H2, at 50-55° C. for 3 h. The mixture was filtered through Celite and the filtrate was concentrated to about 100 mL. The crude was left in the fridge overnight. The solid was filtered and washed with small portion of cold ethanol to afford 4-(3-aminophenoxy)-7-methoxyquinazolin-6-ol (2.05 g, 74.3% yield). 1HNMR (DMSO-d6): δ 10.30 (1H, s), 8.49 (1H, s), 7.46 (1H, s), 7.34 (1H, s), 7.07 (1H, m), 6.48 (1H, m), 6.40 (2H, m), 5.29 (2H, s), 3.90 (3H, s). LC-MS (ESI) m/z 284 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-721b563ef24f47eda9aa5f6d82594160
Source noteuspto-grants-2013_12