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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357278Generated: November 3, 2026

Ammonium Chloride → HCID 178482586, compound

https://huagongshe.com/reaction/1357278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant1-methyl-1H-indole-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amideHCID 12083574—
SolventDimethylformamideHCID 6228—
ProductHCID 178482586HCID 17848258684%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-methyl-1H-indole-3-carboxylic acid (5-bromo-6-cyanomethoxy-naphthalen-2-ylmethyl)-methyl-amide (1.0 g, 2.0 mmol), prepared in the previous step, sodium azide (0.32 g, 6.0 mmol) and ammonium chloride (0.39 g, 6.0 mmol) in 15 mL of DMF was stirred under nitrogen at 100° C. for 6 h. The reaction was partitioned between ethyl acetate and water. The aqueous layer was made basic by the addition of 1 N NaOH. The organic layer was separated and the aqueous layer extracted five times with ethyl acetate. The aqueous layer was then acidified with 1N HCl. After 2 h a white solid had precipitated from solution. The solid was collected by filtration and dried under reduced pressure to give the title compound (0.8460 g, 84%) as an off-white solid, mp 227-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589970B2
Source datasetuspto-grants-2003_07
ORD IDord-f258b715facd431d81a5f5e4808e22e5
Source noteuspto-grants-2003_07