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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097649Generated: October 31, 2026

3-Chloropropanesulphonyl chloride → 3-Chloro-N-({4-[4-(3-chloro-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiaz ol-3-yl}methyl)propane-1-sulfonamide

https://huagongshe.com/reaction/2097649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[4-(Aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4H)-oneHCID 58941843—
SolventDichloromethaneHCID 6344—
Product3-Chloro-N-({4-[4-(3-chloro-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiaz ol-3-yl}methyl)propane-1-sulfonamideHCID 5894178320%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 3-[4-(aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4H)-one (100 mg, 0.32 mol) in DCM (2 mL) under an atmosphere of nitrogen was added DIPEA (168 μL, 0.96 mmol), and 3-chloropropane-1-sulfonyl chloride (117 μL, 0.66 mmol). The reaction was stirred at 25° C. for 5 min. The reaction was quenched with MeOH and purified by preparative HPLC to yield the desired product (38 mg, 20%). 1H NMR (400 MHz, CDCl3): δ 7.5 (m, 1H), 7.3 (m, 2H), 4.8 (d, 2H), 3.7 (t, 2H), 3.25 (t, 2H), 2.3 (m, 2H). MF═C14H12Cl2FN5O5S; LCMS calculated for C14H13Cl2FN5O5S(M+H)+: m/z=452.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450351B2
Source datasetuspto-grants-2013_05
ORD IDord-23120a80c270473c935d4cfb837d8e02
Source noteuspto-grants-2013_05