Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877632Generated: October 25, 2026

3-(Morpholine-4-sulfonyl)benzohydrazide → N-[(E)-1-(5-chloro-2-fluorophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamide

https://huagongshe.com/reaction/877632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Morpholine-4-sulfonyl)benzohydrazideHCID 877246—
Reactant1-(5-Chloro-2-fluorophenyl)ethanoneHCID 2773579—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-[(E)-1-(5-chloro-2-fluorophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamideHCID 8658092019.22%

Reaction Conditions

Temperature120 °C

Reaction Steps

1-(5-chloro-2-fluorophenyl)ethanone (20 mg, 0.116 mmol) and 3-(morpholinosulfonyl)benzohydrazide (33.1 mg, 0.116 mmol) was dissolved in Methanol (Volume: 4 ml) in the presence of acetic acid as a catalyst and then the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Reaction was monitored by TLC. After completion of the reaction, following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) afforded the title compound (E)-N′-(1-(5-chloro-2-fluorophenyl)ethylidene)-3-(morpholinosulfonyl)benzohydrazide (10 mg, 0.022 mmol, 19.22% yield) as a solid. 1H NMR (CDCl3, 400 MHz): δ 8.26 (m, 1H), 8.09 (m, 1H), 7.80 (d, 1H, J=7.6 Hz), 7.58 (t, 1H, J=7.6 Hz), 7.37 (m, 1H), 7.21 (m, 1H), 6.95 (m, 1H), 3.61 (m, 4H), 2.90 (m, 4H), 2.29 (s, 3H). Mass [M+H]+:440.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987335B2
Source datasetuspto-grants-2015_03
ORD IDord-3799ad55235545df8ca98491a57c5750
Source noteuspto-grants-2015_03