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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386281Generated: October 30, 2026

Dimethylformamide → 4-(7-Benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazoline

https://huagongshe.com/reaction/1386281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolineHCID 11823941—
Reactant7-BenzyloxyoxindoleHCID 21717230—
SolventTetrahydrofuranHCID 8028—
Product4-(7-Benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazolineHCID 2171719958.6%

Reaction Steps

Sodium hydride (36 mg, 1.5 mmol) was added in portions to a solution of 7-benzyloxyoxindole (360 mg, 1.5 mmol) in THF (8 ml), the mixture was stirred for 30 minutes at ambient temperature and a solution of 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (204 mg, 0.6 mmol), (prepared as described for the starting material in Example 5), in THF (4 ml) and DMF (1.5 ml) was added. The mixture was stirred for 30 minutes at ambient temperature followed by 1.5 hours at 65° C. The THF was removed by evaporation, the mixture was partitioned between ethyl acetate and water and the aqueous layer was adjusted to pH8 with 2M hydrochloric acid. The precipitated product was collected by filtration, washed with water, ethyl acetate, and ether, and dried under vacuum to give 4-(7-benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazoline (190 mg, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-bf614ded2efb4a0f9632bbb96a78f103
Source noteuspto-grants-2001_07