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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417432Generated: November 1, 2026

Pyridine → HCID 69817752, compound

https://huagongshe.com/reaction/2417432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 69817916HCID 69817916—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 69817752HCID 69817752—

Reaction Steps

To a solution of tert-butyl N-[(1S)-1-[4-[[[(2-aminophenyl)amino]carbonyl]amino]benzyl]-2-hydroxyethyl]-N-[(2S)-2-hydroxy-3-phenoxypropyl]carbamate (20.0 mg) in 1,2-dichloroethane (200 μl) were added successively 1.0 M solution of pyridine in 1,2-dichloroethane (54.5 μl) and 1.0 M solution of methanesulfonyl chloride in 1,2-dichloroethane (43.6 μl) at room temperature. After stirring for 2 hours, the solvent was removed by evaporation and the residue was purified by a recycling preparative high pressure liquid chromatography equipped with a gel permeation chromatography column (eluent: chloroform) to give a light brown solid. The solid was dissolved in 1,2-dichloroethane (200 μl). To the solution was added trifluoroacetic acid (200 μl) and the mixture was stirred for 30 minutes. The solvent was removed by evaporation to give N-[2-[[[[4-[(2S)-3-hydroxy-2-[[(2S)-2-hydroxy-3-phenoxypropyl]amino]propyl]phenyl]amino]-carbonyl]amino]phenyl]methanesulfonamide trifluoroacetate (20.3 mg) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06826033B2
Source datasetuspto-grants-2004_11
ORD IDord-cc4739433c884bf6b2495586a443708a
Source noteuspto-grants-2004_11