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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791577Generated: November 4, 2026

2,3-dimethyl-1H-indol-5-amine → 4(2,3-Dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochloride

https://huagongshe.com/reaction/1791577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-dimethyl-1H-indol-5-amineHCID 258688—
Reactant4-Chloro-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazolineHCID 11141792—
Product4(2,3-Dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochlorideHCID 2203095476.3%

Reaction Steps

Using an analogous procedure to that described in Example 37, 4-chloro-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline (100 mg, 0.31 mmol), (prepared as described for the starting material in Example 9), was reacted with 5-amino-2,3-dimethylindole (55 mg, 0.34 mmol) to give 4(2,3-dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochloride (114 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-a64612f1488145b3a1017e0a6b4aac55
Source noteuspto-grants-2006_07