HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845779Generated: October 30, 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/1845779
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-[4-(Aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4H)-one | HCID 58941843 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 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 | HCID 58941783 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08951536B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-a930f7221ad34b62a88ecacc815ffa46 |
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| Source note | uspto-grants-2015_02 |
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