Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloroacetamidine monohydrochloride | HCID 2776957 | — |
| Reactant | HCID 178418558 | HCID 178418558 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178512424 | HCID 178512424 | 36.7% |
Reaction Steps
To a solution of 1.50 g of 2,5-dimercapto-1,3,4-thiadiazole and 4.2 ml of triethylamine in 30 ml of DMF was added 1.29 g of α-chloroacetamidine hydrochloride at room temperature under stirring. Further, the mixture was stirred for 2.5 hours at room temperature and concentrated under reduced pressure. The residue was subjected to a column chromatography on silica gel (100 g), eluting with a (4:1) mixture of acetonitrile and water. The pertinent fractions were collected and concentrated under reduced pressure, and the concentrate was subjected to a column chromatography on XAD-II (450 ml) being washed with water, and eluted with 10% aqueous ethanol. After concentrating, the precipitating crystals were filtered to give 755mg of 2-amidinomethylthio-5-mercapto-1,3,4-thiadiazole as colorless crystals, mp: 184°-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04971963 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-7931e3afdf424e2a9c8b6c6f4e805a7c |
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| Source note | uspto-grants-1990_11 |
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