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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61666Generated: October 29, 2026

4-Chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazoline → HCID 59361995, compound

https://huagongshe.com/reaction/61666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazolineHCID 59361897—
Reactant5-amino-1H-indazole-1-carboxylateHCID 86642411—
SolventIsopropanolHCID 3776—
ProductHCID 59361995HCID 59361995149.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 4-chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazoline (0.500 g, 1.28 mmol) and 5-amino-1H-indazole-1-carboxylate (0.314 g, 1.34 mmol) in iso-propanol (30 mL) was heated at 95° C. for 30 minutes and at 95° C. for 8 h. The mixture was allowed to cool to RT and the solid was collected via filtration. The cake was washed with iso-propanol and Et2O, triturated with CH2Cl2 and EtOAc and dried in vacuo to give tert-Butyl 5-(7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (0.560 g, 0.955 mmol, 71%). MS 587 (M+1). HPLC retention time 7.21 mins.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440961B2
Source datasetuspto-grants-2016_09
ORD IDord-285c7538f9964a96a8c51fcc274aee98
Source noteuspto-grants-2016_09