HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286982Generated: October 30, 2026
Bromine → Methyl 5-amino-1,2,4-thiadiazole-3-carboxylate
https://huagongshe.com/reaction/2286982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-Ethoxycarbonylformamidine hydrobromide | HCID 23316851 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-amino-1,2,4-thiadiazole-3-carboxylate | HCID 13577102 | 67.8% |
Reaction Steps
To a solution of 1-ethoxycarbonylformamidine. hydrobromide (16.6 g.) in absolute methanol (84 ml) was added a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. To the mixture were added alternately bromine (12.8 g) and a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. and then to the suspension was added potassium thiocyanate (8.1 g) in absolute methanol (100 ml). The reaction mixture was stirred for an hour at 0° C. and for an additional 6 hours at ambient temperature. The mixture was filtered through cellulose powder and the filtrate was evaporated to dryness. The residue was dissolved in a mixture of ethyl acetate and water, and then the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was triturated with diethyl ether to give the title compound (9.0 g), mp. 202° to 205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04268509 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-18412570489a481fa99941b017428ac0 |
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| Source note | uspto-grants-1981_05 |
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