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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357257Generated: November 2, 2026

Sodium Hydroxide → 2-Ethyl-benzofuran-3-carboxylic acid [5-bromo-6-(1H-tetrazol-5-ylmethoxy)-naphthalen-2-ylmethyl]-methyl-amide

https://huagongshe.com/reaction/1357257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant2-Ethyl-benzofuran-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amideHCID 12083569—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Ethyl-benzofuran-3-carboxylic acid [5-bromo-6-(1H-tetrazol-5-ylmethoxy)-naphthalen-2-ylmethyl]-methyl-amideHCID 17843809456%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-ethyl-benzofuran-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amide (0.25 g, 0.5237 mmol), prepared in the previous step, sodium azide (0.10 g, 1.57 mmol) and ammonium chloride (0.084 g, 1.57 mmol) in 12 mL DMF was stirred under nitrogen at 100° C. for 5 h. The reaction was diluted with water, made basic with 1N NaOH and extracted four times with ethyl acetate. The combined organic extracts were acidified with 1N HCl, the solvent removed under reduced pressure and the resulting residue diluted with water. The solid foam that formed was collected by filtration and dried under reduced pressure to give the title compound (0.15 g, 56%) as a tan foam, MS m/z: 520 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589970B2
Source datasetuspto-grants-2003_07
ORD IDord-612cb19ac455486a94daeacf2a47f4e8
Source noteuspto-grants-2003_07