HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080723Generated: October 27, 2026
1-Hydroxybenzotriazole → t-Butyl[4-(5-cyano-2-propylaminophenylcarbamoyl)butyl]carbamate
https://huagongshe.com/reaction/2080723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 5-(((Tert-butoxy)carbonyl)amino)pentanoic acid | HCID 545848 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-Amino-4-(propylamino)benzonitrile | HCID 22380299 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | t-Butyl[4-(5-cyano-2-propylaminophenylcarbamoyl)butyl]carbamate | HCID 21084519 | 99.9% |
Reaction Steps
In chloroform (31 ml), 5-t-butoxycarbonylamino valeric acid (1.57 g), WSCI hydrochloride (1.98 g), and HOBt (1.39 g) were dissolved. Then, the solution was stirred at room temperature for 30 minutes. The solution was dropped in a chloroform solution (10 ml) containing the compound (1.18 g) obtained in Example 5-2. Then, the whole was stirred at room temperature for 12 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform and then washed with a saturated aqueous sodium hydrogen carbonate solution, a saturated aqueous ammonium chloride solution, and a saturated saline solution, followed by drying with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure and the residue was then purified through silica gel column chromatography (chloroform/ethyl acetate) to remove only highly-polar components, thereby obtaining a mixture (2.52 g) containing the subject compound as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932281B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-1cfa19c5714544cfbb96f64860efe47b |
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| Source note | uspto-grants-2011_04 |
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