Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378002Generated: October 31, 2026

Methylamine → HCID 54132471, compound

https://huagongshe.com/reaction/1378002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 54171952HCID 54171952—
SolventEthanolHCID 702—
ProductHCID 54132471HCID 54132471100%

Reaction Steps

5.3 g (10.2 mmol) of (S)-8-trifluoromethyl-12,12a-dihydro-1-(3-phthalimidomethyl-1,2,4-oxadiazol-5-yl)-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one in 70 ml of ethanol were treated dropwise with 150 ml of methylamine (33% in ethanol) at 60° within 45 min. The solution was stirred at 70° for 2 hours and subsequently concentrated. The residue was taken up in methylene chloride and 30 ml of 4N hydrochloric acid and the solution was washed three times with methylene chloride. The aqueous phase was made alkaline with 30 ml of 4N sodium hydroxide solution and extracted five times with methylene chloride. After drying the combined organic solutions and evaporating the solvent there were obtained 3.98 g (100%) of (S)-1-(3-aminomethyl-1,2,4-oxadiazol-5-yl)-8-trifluoromethyl-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was used without further purification as the starting material for the Example described hereinafter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-bcdb47f636834c8e8bcebec09b4fe628
Source noteuspto-grants-1997_09