HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711006Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 117988560, compound
https://huagongshe.com/reaction/711006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Benzyl (2-(aminooxy)ethyl)carbamate | HCID 13983481 | — |
| Reactant | HCID 89423114 | HCID 89423114 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117988560 | HCID 117988560 | 100% |
Reaction Steps
(2S,5R)-5-((Benzyloxy)amino)-1-(tert-butoxycarbonyl)piperidine-2-carboxylic acid (1.879 g, 5.362 mmol) described in Example 99 or 100, benzyl 2-(aminooxy)ethylcarbamate (1.41 g, 6.707 mmol) of Reference Example 11 and 1-hydroxybenzotriazole.monohydrate (220 mg) were dissolved in methylene chloride (20 mL), followed by stirring under ice cold. To this was added N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.29 g), and a temperature was elevated to room temperature, followed by stirring overnight. The mixture was diluted with methylene chloride (20 mL), and washed with water, 10% citric acid aqueous solution, saturated sodium bicarbonate aqueous solution, and saturated brine sequentially, and then dried over magnesium sulfate. The solvent was concentrated under reduced pressure to afford 2.91 g of the title compound (quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181250B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-a6360c89da70422aaddf8d2ffba6300a |
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| Source note | uspto-grants-2015_11 |
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