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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tripropylamine | HCID 7616 | — |
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 1-(4-Methoxy-benzenesulfonyl)-2,3,4,7-tetrahydro-1H-azepine-2,3-dicarboxylic acid 2-tert-butyl ester | HCID 15550523 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(3,3-Dibenzylureido)-1-(4-methoxy-benzenesulfonyl)-2,3,4,7-terahydro-1H-azepine-2-carboxylic acid | HCID 12087867 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838454B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-39772fbca4e6434ba996bc2fd06b0adb |
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| Source note | uspto-grants-2005_01 |
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