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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131889Generated: October 30, 2026

Pyridine → HCID 59732931, compound

https://huagongshe.com/reaction/131889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59732818HCID 59732818—
SolventDichloromethaneHCID 6344—
ProductHCID 59732931HCID 5973293175%

Reaction Steps

To 1-[4-(amino-ethyl)-thiazol-2-yl]-3-(2-cyclopentanecarbonyl-4-methyl-phenyl)-urea (0.05 g, 0.13 mmol) in 10 mL DCM at 0° C. was added methanesulfonyl chloride (0.02 g, 0.13 mmol) followed by pyridine (0.02 g, 0.21 mmol). The reaction was stirred at ambient temperature overnight, concentrated and purified by flash chromatography on silica gel with 20–50% EtOAc/hexane to obtain the product as white solid in 75% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384967B2
Source datasetuspto-grants-2008_06
ORD IDord-45ac53bf3c8d4efa8a1f7a6754bde5c8
Source noteuspto-grants-2008_06