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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386244Generated: November 1, 2026

N-Methyloxindole → HCID 21717225, compound

https://huagongshe.com/reaction/1386244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethyloxindoleHCID 6096—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21717225HCID 2171722520.5%

Reaction Steps

Potassium bis(trimethylsilyl)amide (5 ml of a 0.5M solution in toluene, 2.5 mmol) was rapidly added at ambient temperature to a solution of 4-chloro-6,7-dimethoxyquinazoline (337 mg, 1.5 mmol) and 1-methyloxindole (368 mg, 2.5 mmol), (prepared according to the method described in J. Am. Chem. Soc 1945, 67, 1656), in THF (30ml). After 30 minutes, the precipitate was collected by filtration and washed with ether. A second precipitate was isolated from the filtrate. The two solids were mixed and purified by column flash chromatography using methylene chloride/methanol (96/4 and 94/6) as eluent. During the evaporation of the solvents, the compound crystallised. The solid was filtered off, washed with ether and dried under vacuum to give 6,7-dimethoxy-4-(1-methyloxindol-3-yl)quinazoline (103 mg, 20%) as red orange needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-516bde44ce12400eb47b4ed2f340a271
Source noteuspto-grants-2001_07