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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565061Generated: October 31, 2026

Stannous chloride dihydrate → Ethyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylate

https://huagongshe.com/reaction/565061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 21194161HCID 21194161—
SolventEthanolHCID 702—
ProductEthyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylateHCID 2119443371.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4.10 g (10.9 mmol) of ethyl 4-chloro-1-methyl-7-(4-nitrophenoxy)-2-indolecarboxylate, 12.34 g (54.7 mmol) of tin (II) chloride dihydrate and 150 ml of ethanol was stirred at 70° C. for 3 hours. After the reaction mixture was cooled to room temperature, 28% ammonia water was added to render alkaline and the mixture was extracted with ethyl acetate. Insoluble matters were filtered off. The filtrate was washed with 5% sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 2.70 g of ethyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-e8598d7f8f0a453aae2910b5a19101a7
Source noteuspto-grants-2001_01