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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386355Generated: October 29, 2026

Sodium hydride → HCID 21717295, compound

https://huagongshe.com/reaction/1386355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-methyl-2-oxoindoline-5-sulfonamideHCID 10176909—
Reactant4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolineHCID 11823941—
SolventDimethylformamideHCID 6228—
ProductHCID 21717295HCID 2171729554.1%

Reaction Steps

A solution of 5-methylaminosulphonyloxindole (262 mg, 1.16 mmol) in DMF (3.5 ml) was added dropwise to a suspension of sodium hydride (46 mg, 1.1 6 mmol, prewashed with hexane) in DMF (1.5 ml). The mixture was stirred for 30 minutes at ambient temperature and 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (130 mg, 0.38 mmol), (prepared as described for the starting material in Example 5), was added as a solid. The mixture was stirred for 45 minutes at 60° C. and was then partitioned between ether and water. The aqueous layer was separated and was adjusted to pH7-8 with 1M hydrochloric acid. The precipitate was collected by filtration, washed with water and ether, and dried under vacuum. The solid was suspended in methylene chloride/methanol (1/1) and 2.2M ethereal hydrogen chloride (1.5 ml) was added. The mixture was stirred for 10 minutes at ambient temperature and the volatiles were removed by evaporation. The solid residue was triturated with ether, collected by filtration, washed with ether and dried under vacuum at 60° C. to give 6-methoxy-4-(5-methylaminosulphonyloxindol-3-yl)-7-(3-morpholinopropoxy)quinazoline hydrochloride (116 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-9d96f600e63c4359a811d1f65b922d77
Source noteuspto-grants-2001_07