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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558969Generated: October 30, 2026

Ammonium Chloride → HCID 178426906, compound

https://huagongshe.com/reaction/558969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant4-Cyanomethyl-8-fluoro-3-oxo-3,4-dihydro-2H-quinoxaline-1-carboxylic acid 2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)benzylamideHCID 11584492—
SolventDimethylformamideHCID 6228—
ProductHCID 178426906HCID 178426906—

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium azide (78 mg, 1.2 mmol) and ammonium chloride (21 mg, 0.40 mmol) were added to a solution of 4-cyanomethyl-8-fluoro-3-oxo-3,4-dihydro-2H-quinoxaline-1-carboxylic acid 2-methyl-4-(2,3,4,5-tetrahydrobenzo[b]azepine-1-carbonyl)benzylamide from Example 13 (210 mg, 0.40 mmol) in DMF (5 ml) and the mixture was stirred at 100° C. for 18 h. The mixture was cooled and evaporated in vacuo. The residue was purified by flash chromatography on silica (eluant CHCl3 100% to CHCl3:methanol;triethylamine 97:2:1 to CHCl3:methanol;triethylamine 94:4:2). The product was partitioned between chloroform and potassium hydrogen sulphate, separated and the organic phase was dried and evaporated in vacuo; yield 33 mg, 15%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063038B2
Source datasetuspto-grants-2011_11
ORD IDord-8f6b48b1178a430aaba52428b526211f
Source noteuspto-grants-2011_11