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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278034Generated: October 25, 2026

Diisopropylamine → HCID 178509145, compound

https://huagongshe.com/reaction/278034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
Reactant5-(1-Amino-3-phenylpropyl)-[1,3,4]oxadiazol-2-ylamineHCID 22626939—
ReactantHCID 178524160HCID 178524160—
SolventDimethylformamideHCID 6228—
ProductHCID 178509145HCID 178509145—

Reaction Steps

0.18 g of 5-(1-amino-3-phenylpropyl)-[1,3,4]oxadiazol-2-ylamine was dissolved in 10 ml of dry dimethylformamide at RT, treated with 200 mg of 2-pyridin-4-yl-1H-benzimidazole-5-carboxylic acid, 270 mg of TOTU, and 0.12 ml of diisopropylamine, and stirred at RT for 4 h. The reaction mixture was concentrated, and the residue was taken up in ethyl acetate and washed successively with water, saturated sodium hydrogencarbonate solution, water, and saturated sodium chloride solution. The organic phase was dried over magnesium sulfate, filtered, and concentrated. The residue was stirred with methyl tert-butyl ether, filtered off, and dried under high vacuum. 2-Pyridin4-yl-1H-benzimidazole-5-carboxylic acid [1-(5-amino-[1,3,4]oxadiazol-2-yl)-3-phenylpropyl]amide, which melts at 160° C. with decomposition, is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358978B1
Source datasetuspto-grants-2002_03
ORD IDord-f71fbc6784cd47cc9dde6ac5c08115e2
Source noteuspto-grants-2002_03