HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543829Generated: October 31, 2026
Dichloromethane → HCID 14769542, compound
https://huagongshe.com/reaction/543829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| Reactant | Methyl 5-formamido-1,2,4-thiadiazole-3-carboxylate | HCID 13577103 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14769542 | HCID 14769542 | 32.8% |
Reaction Steps
To a mixture of methyl 5-formamido-1,2,4-thiadiazole-3-carboxylate (9.2 g) and methyl methylthiomethyl sulfoxide (6.1 g) in N,N-dimethylformamide (100 ml) was added 50% sodium hydride (7.1 g) with cooling in an ice-bath. The mixture was stirred for an hour at ambient temperature and for an additional one hour at 40° C. After cooling to ambient temperature, methylene chloride (300 ml) was added to the reaction mixture, and the resulting precipitates were collected by filtration and washed with methylene chloride. The precipitates were added to a stirred mixture of hydrochloric acid (14.7 ml), ice-water (200 ml) and methylene chloride (200 ml). An insoluble material was filtered off and the methylene chloride layer was separated from the filtrate. The solution was dried over anhydrous magnesium sulfate, evaporated and the residue was triturated with diethyl ether to give the title compound (4.5 g), mp. 130° to 132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04447429 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-1c26e8c4dfa44530abddd4286b6a7bc9 |
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| Source note | uspto-grants-1984_05 |
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