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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793832Generated: November 3, 2026

Tripropylamine → 3-(3,3-Dibenzylureido)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic Acid tert-butyl Ester

https://huagongshe.com/reaction/1793832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTripropylamineHCID 7616—
ReactantDibenzylamineHCID 7656—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl esterHCID 15550523—
Solvent1,4-DioxaneHCID 31275—
Product3-(3,3-Dibenzylureido)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2-carboxylic Acid tert-butyl EsterHCID 12087866—

Reaction Conditions

Temperature75 °C

Reaction Steps

The reaction is performed under an Argon blanket. 1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl ester (204 mg, 0.5 mmol) is dissolved in 10 ml dry Dioxane. Tripropylamine (94 μl, 0.5 mmol) is added and then Diphenyl phosphoryl azide (DPPA). The reaction is heated to 75° C. for 5 h. After cooling to room temperature, Dibenzylamine (190.6 μl, 1 mmol) is added via syringe. The reaction is heated to 70° C. and stirred over night. Evaporation of the solvents and flash-chromatography, Hexane/Ethyl acetate (1:1) afforded the product: Cal. 606.8 found (M)+ 606.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022690B2
Source datasetuspto-grants-2006_04
ORD IDord-99da9018331d4c898c6972eaa71da694
Source noteuspto-grants-2006_04