HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080715Generated: October 27, 2026
1-Hydroxybenzotriazole → Methyl 4-(5-t-butoxycarbonylamino-pentanoylamino)-3-propylamino-benzoate
https://huagongshe.com/reaction/2080715
Participants
| Role | Name | HCID | Charge |
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| 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 | Methyl 4-amino-3-(propylamino)benzoate | HCID 23155569 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 4-(5-t-butoxycarbonylamino-pentanoylamino)-3-propylamino-benzoate | HCID 23155436 | 54.9% |
Reaction Steps
In chloroform (10 ml), 5-t-butoxycarbonylamino valeric acid (574 mg), WSCI hydrochloride (690 mg), and HOBt (487 mg) were dissolved. Then, the solution was stirred at room temperature for 30 minutes. The solution was added with the compound (503 mg) obtained in Example 3-1 and stirred overnight at room temperature. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was then dissolved in chloroform. After having been washed with a saturated aqueous sodium hydrogen carbonate solution, a saturated aqueous ammonium chloride solution, and a saturated saline solution, the resultant was dried 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), thereby obtaining the subject compound (540 mg) as a colorless viscous 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-5e352287d3f04e45a126f9644e77ddcf |
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| Source note | uspto-grants-2011_04 |
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