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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917719Generated: October 26, 2026

1-(5-Tert-butylisoxazol-3-yl)-3-(3-hydroxyphenyl)urea → 1-(5-Tert-butylisoxazol-3-yl)-3-(3-(6-(2-methoxyethoxy)quinazolin-4-yloxy)phenyl)urea

https://huagongshe.com/reaction/1917719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Tert-butylisoxazol-3-yl)-3-(3-hydroxyphenyl)ureaHCID 66876595—
Reactant4-Chloro-6-(2-methoxyethoxy)quinazolineHCID 86650899—
Product1-(5-Tert-butylisoxazol-3-yl)-3-(3-(6-(2-methoxyethoxy)quinazolin-4-yloxy)phenyl)ureaHCID 5826789920%

Reaction Steps

The title compound was prepared from 1-(5-tert-butylisoxazol-3-yl)-3-(3-hydroxyphenyl)urea from Example 1A (138 mg, 0.5 mmol) and 4-chloro-6-(2-methoxyethoxy)quinazoline from Example 40A Step 5 (119 mg, 0.5 mmol) using the procedure of Example 16C. The crude product was purified by column chromatography (25-100% EtOAc/hexanes) to give 1-(5-tert-butylisoxazol-3-yl)-3-(3-(6-(2-methoxyethoxy)quinazolin-4-yloxy)phenyl)urea (45 mg, 0.094 mmol, 20%). 1H NMR (300 MHz, DMSO-d6) δ 9.59 (s, 1H), 9.01 (s, 1H), 8.62 (s, 1H), 7.94 (d, 1H), 7.74-7.64 (m, 3H), 7.60 (s, 1H), 7.42 (t, 1H), 7.27 (d, 1H), 6.99 (d, 1H), 6.48 (s, 1H), 4.37-4.31 (m, 2H), 3.78-3.71 (m, 2H), 3.34 (s, 3H), 1.28 (s, 9H); LC-MS (ESI) m/z 478 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-9688df6930a349f085f1a5873b2a43fc
Source noteuspto-grants-2013_12