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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759689Generated: November 2, 2026

Tripropylamine → 3-(3,3-Dibenzylureido)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-terahydro-1H-azepine-2-carboxylic acid

https://huagongshe.com/reaction/1759689

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-terahydro-1H-azepine-2-carboxylic acidHCID 12087867—

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 numberUS06838454B2
Source datasetuspto-grants-2005_01
ORD IDord-39772fbca4e6434ba996bc2fd06b0adb
Source noteuspto-grants-2005_01