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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917694Generated: October 30, 2026

4-Chloro-6-(3-chloropropoxy)-7-methoxyquinazoline → 1-(5-Tert-butylisoxazol-3-yl)-3-(3-(6-(3-chloropropoxy)-7-methoxyquinazolin-4-yloxy)phenyl)urea

https://huagongshe.com/reaction/1917694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-(3-chloropropoxy)-7-methoxyquinazolineHCID 50742264—
Reactant1-(5-Tert-butylisoxazol-3-yl)-3-(3-hydroxyphenyl)ureaHCID 66876595—
Product1-(5-Tert-butylisoxazol-3-yl)-3-(3-(6-(3-chloropropoxy)-7-methoxyquinazolin-4-yloxy)phenyl)ureaHCID 6687580355%

Reaction Steps

1-(5-tert-butylisoxazol-3-yl)-3-(3-hydroxyphenyl)urea from Example 1A (1.92 g, 6.97 mmol) and 4-chloro-6-(3-chloropropoxy)-7-methoxyquinazoline from the previous step (2.0 g, 6.97 mmol) were reacted in the manner described in Example 16C to give 1-(5-tert-butylisoxazol-3-yl)-3-(3-(6-(3-chloropropoxy)-7-methoxyquinazolin-4-yloxy)phenyl)urea (2.00 g, 3.8 mmol, 55%). 1H NMR (300 MHz, DMSO-d6) δ 9.56 (s, 1H), 8.98 (s, 1H), 8.54 (s, 1H), 7.59 (s, 1H), 7.54 (s, 1H), 7.38 (t, 1H), 7.33 (s, 1H), 7.26 (d, 1H), 6.96 (d, 1H), 6.47 (s, 1H), 4.27 (t, 2H), 3.98 (s, 3H), 3.82 (t, 2H), 2.30-2.24 (m, 2H), 1.29 (s, 9H); LC-MS (ESI) m/z 526 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-3f3cd3d882a247ac907015bace48d6c6
Source noteuspto-grants-2013_12