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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097653Generated: October 30, 2026

Methanesulfonyl chloride → HCID 178505093, compound

https://huagongshe.com/reaction/2097653

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-aminoethyl)-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 numberUS08450351B2
Source datasetuspto-grants-2013_05
ORD IDord-7d697205ca9a4587a00d10cb1f23f132
Source noteuspto-grants-2013_05