Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Carbonimidic acid, N-cyano-, dimethyl ester | HCID 90604 | — |
| Reactant | HCID 178512678 | HCID 178512678 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178485071 | HCID 178485071 | — |
Reaction Steps
Pure 3-chloromethyl-5-guanidino-1,2,4-thiadiazole (150 g.) was stirred in ethanol (600 ml.) at 10° and 2-aminoethanethiol hydrochloride (93 g.) added. 18 N NaOH (92 ml.) diluted with water (300 ml.) was then added over 30 minutes at 10°-15°. After 90 minutes further water (600 ml.) was added and the solution was stirred for a further 30 minutes before dimethyl (N-cyanoimido)carbonate (107 g.) was added. The resulting solution was stirred for 60 minutes and then aqueous methylamine (40% w/w, 660 ml.) was added. The mixture was stirred for 18 hours and the product removed by filtration and washed with ethanol/water (1:1 v/v, 2×250 ml.) (164 g., 67%). Crystallisation from ethanol/water 3:1 v/v gave 3-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]-5-guanidino-1,2,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04242350 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-11759cc192a64d8bba78c504dc077e49 |
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| Source note | uspto-grants-1980_12 |
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