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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602508Generated: October 30, 2026

Ammonium Chloride → HCID 178441410, compound

https://huagongshe.com/reaction/1602508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantSodium BisulfateHCID 516919—
ReactantHCID 19611382HCID 19611382—
SolventDimethylformamideHCID 6228—
ProductHCID 178441410HCID 17844141074%

Reaction Conditions

Temperature70 °C

Reaction Steps

Dimethylformamide (13 ml) was added to a mixture of 3-[(4-tert-butyl-2-thiazolyl)methoxy]-5'-[3-(4-chlorophenylsulfonyl)propyl]-2'-cyanomethoxybenzanilide (1.30 g, 2.04 mmol), ammonium chloride (0.20 g, 4.08 mmol) and sodium azide (0.25 g, 4.08 mmol), and the resulting mixture was stirred at 70° C. for 12 hours. Ice and 5% sodium hydrogensulfate aqueous solution were added to the reaction solution and the product formed was extracted with ethyl acetate. The resulting organic layer was washed with water and brine in that order, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (eluent=methanol:chloroform=5:100) and then crystallized from acetonitrile to give 3-[(4-tert-butyl-2-thiazolyl)methoxy]-5'-[3-(4-chlorophenylsulfonyl)propyl]-2'-(1H-tetrazol-5-ylmethoxy)benzanilide (1.02 g, 74%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981559
Source datasetuspto-grants-1999_11
ORD IDord-2f4aee6251694bf883014b827b5c5560
Source noteuspto-grants-1999_11