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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417449Generated: November 1, 2026

HCID 69818043, compound → HCID 69818012, compound

https://huagongshe.com/reaction/2417449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69818043HCID 69818043—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 69818012HCID 6981801220%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06826033B2
Source datasetuspto-grants-2004_11
ORD IDord-b0bd0d9210894543a8c7d7f880230e0d
Source noteuspto-grants-2004_11