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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108063Generated: October 30, 2026

Dipropylamine → HCID 15106962, compound

https://huagongshe.com/reaction/2108063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 14699764HCID 14699764—
SolventDimethylformamideHCID 6228—
ProductHCID 15106962HCID 15106962—

Reaction Steps

To a solution of 1.1 g of 3-[4-(2-chlorophenyl)-6,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl]propionic acid in 15 ml of dimethylformamide are added 0.4 g of N-hydroxybenzotriazole and 0.4 ml of dipropylamine and stirred at room temperature for 10 minutes. To the mixture is added 0.65 g of dicyclohexyl carbodiimide under ice-cooling and stirred for 4 hours and furthermore stirred at room temperature for 16 hours. The resulting dicyclohexylurea is filtered off and to the filtrate is added 50 ml of chloroform. The solution is washed with 5% aqueous sodium hydrogencarbonate solution and water and dried over anhydrous magnesium sulfate. After separating by filtration, the filtrate is concentrated under reduced pressure and the residue is subjected to chromatography on silica gel and then eluted with a mixture of chloroform-methanol (100:1 to 100:3). The eluate of the objective fraction is concentrated under reduced pressure to give 1 g of 3-[4-(2-chlorophenyl)-6,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl]propionic acid N,N-dipropylamide as pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937240
Source datasetuspto-grants-1990_06
ORD IDord-87fe0ff6eafb4ddd8f4fa2c5a7eb8e4e
Source noteuspto-grants-1990_06