HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417449Generated: November 1, 2026
HCID 69818043, compound → HCID 69818012, compound
https://huagongshe.com/reaction/2417449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69818043 | HCID 69818043 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69818012 | HCID 69818012 | 20% |
Reaction Steps
In 4N hydrogen chloride in ethanol (2.0 ml), tert-butyl N-[(2S)-2-hydroxy-3-phenoxypropyl]-N-[(1S)-2-hydroxy-1-[4-[(1H-pyrrol-3-ylcarbonyl)amino]benzyl]ethyl]carbamate (113.5 mg) was dissolved and the solution was stirred at room temperature for 30 hours. After concentration under reduced pressure, the residue was extracted with ethyl acetate (20 ml) and washed with saturated sodium hydrogencarbonate aqueous solution (20 ml). The organic layer was separated and the aqueous layer was extracted twice with ethyl acetate (20 ml). The organic layers were combined and washed with brine, and dried over magnesium sulfate to give N-[4-[(2S)-3-hydroxy-2-[[(2S)-2-hydroxy-3-phenoxypropyl]amino]propyl]-phenyl]-1H-pyrrole-3-carboxamide (18.2 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06826033B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-b0bd0d9210894543a8c7d7f880230e0d |
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| Source note | uspto-grants-2004_11 |
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