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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845782Generated: November 1, 2026

Methanesulfonyl chloride → HCID 178505093, compound

https://huagongshe.com/reaction/1845782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 69268230HCID 69268230—
SolventDichloromethaneHCID 6344—
ProductHCID 178505093HCID 178505093100.9%

Reaction Steps

To a solution of 3-[4-(2-amino ethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4H)-one trifluoroacetate (16.0 mg, 0.037 mmol) in DCM (1.0 mL) was added TEA (15 μL, 0.11 mmol) and methanesulfonyl chloride (4.2 μL, 0.055 mmol). The resulting mixture was stirred at rt for 1 h and then the solvent was removed under reduced pressure. The residue was dissolve in MeOH (1 mL) and 2.0 M sodium hydroxide in water (0.10 mL) was added. After stirring for 4 h, the reaction solution was diluted with MeOH and a few drop of acetic acid and then purified by preparative LCMS to give the desired product as a white solid (14.1 mg, 78.3%). MF=C12H13ClFN5O4S; LCMS calculated C12H14ClFN5O4S (M+H)+: m/z=377.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951536B2
Source datasetuspto-grants-2015_02
ORD IDord-0946af3565cf4e74bc15c736c6f46187
Source noteuspto-grants-2015_02