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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855735Generated: October 25, 2026

5-(4-Methoxyphenyl)-2,4-dihydro-3H-pyrazol-3-one → 4-(5-(4-Methoxyphenyl)pyrazol-3-yloxy)-6-methoxy-7-(3-methylsulphonylpropoxy)quinazoline

https://huagongshe.com/reaction/855735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Methoxyphenyl)-2,4-dihydro-3H-pyrazol-3-oneHCID 605366—
Reactant4-Chloro-6-methoxy-7-(3-methylsulphonylpropoxy)quinazolineHCID 21874823—
Product4-(5-(4-Methoxyphenyl)pyrazol-3-yloxy)-6-methoxy-7-(3-methylsulphonylpropoxy)quinazolineHCID 1794275391%

Reaction Steps

Using a procedure analogous to that described in Example 34, 4-chloro-6-methoxy-7-(3-methylsulphonylpropoxy)quinazoline (150 mg, 0.45 mol) was reacted with 3-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-5-one (105 mg, 0.54 mol), (prepared as described for the starting material in Example 10), to give 4-(5-(4-methoxyphenyl)pyrazol-3-yloxy)-6-methoxy-7-(3-methylsulphonylpropoxy)quinazoline (220 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262201B1
Source datasetuspto-grants-2007_08
ORD IDord-1026d0db501a4c5b91c8434fb57d292b
Source noteuspto-grants-2007_08