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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845746Generated: November 1, 2026

Methanesulfonyl chloride → HCID 178505112, compound

https://huagongshe.com/reaction/1845746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58941938HCID 58941938—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 178505112HCID 1785051126.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

4-(3-Chloro-4-fluorophenyl)-3-(4-[(2-morpholin-4-ylethyl)amino]methyl-1,2,5-oxadiazol-3-yl)-1,2,4-oxadiazol-5(4H)-one (20 mg, 0.047 mmol) was dissolved in anhydrous ACN (200 μL) followed by addition of DIPEA (40 μL, 0.2 mmol) and methanesulfonyl chloride (4.0 μL, 0.052 mmol). The reaction was stirred at 40° C. for 2 hrs. The reactions was then diluted with MeOH and purified by HPLC. The purified fractions were concentrated to dryness, redissolved in EtOH (1 mL) and 2 M of sodium hydroxide in water (0.26 mL) was added. The reaction was stirred at rt for 2 hrs, quenched with acetic acid, diluted with MeOH and purified by preparative LCMS to afford the desired product (1.4 mg). MF=C17H22ClFN6O5S; LCMS calculated for C17H23ClFN6O5S(M+H)+: m/z=477.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951536B2
Source datasetuspto-grants-2015_02
ORD IDord-12443dd98300441099c73949cba6b3a3
Source noteuspto-grants-2015_02