HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699653Generated: October 26, 2026
Dichloromethane → 4-methyl-N-(4-methylphenyl)-N-morpholinothio-1,2,3-thiadiazole-5-carboxamide
https://huagongshe.com/reaction/1699653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-methyl-N-(4-methylphenyl)-1,2,3-thiadiazole-5-carboxamide | HCID 850826 | — |
| Reactant | 4-Morpholinesulfenyl chloride | HCID 12297779 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-methyl-N-(4-methylphenyl)-N-morpholinothio-1,2,3-thiadiazole-5-carboxamide | HCID 15906625 | 52% |
Reaction Steps
To 10 ml of methylene chloride were added 0.50 g (2.1 mmol) of 4-methyl-N-(4-methylphenyl)-1,2,3-thiadiazole-5-carboxamide and 0.50 g (3.3 mmol) of N-(chlorosulfenyl)morpholine. Then, 0.33 g (3.3 mmol) of triethylamine was slowly added thereto, and the resulting mixture was reacted with stirring for 5 hours. After the reaction was completed, the reaction mixture containing the objective product was poured into water, the objective product was extracted with ethyl acetate, the organic layer was washed with water and dried on anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the crude crystal thus obtained was washed with ether. As a result, 0.38 g of the objective compound was obtained (Property: m.p. 60° C. (decomposed); Yield: 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06348460B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-9cc0f3aa999e4288ac25e7d0812b3bd0 |
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| Source note | uspto-grants-2002_02 |
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