Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 14456838 | HCID 14456838 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14456840 | HCID 14456840 | 87.8% |
Reaction Steps
To 20 ml of 3 N-hydrochloric acid is added 2.94 g of 6-(2-tert-butoxycarbonylaminoethylthio)imidazo[1,2-b]pyridazine and the mixture is stirred at room temperature for 1.5 hours. Then, a solution of 4.06 g of potassium cyanate in 40 ml of water is added dropwise over 15 minutes with stirring at 35° C. and the mixture is further stirred at the same temperature for 1 hour and at 60° C. for 1 hour. To the reaction mixture are added 2.5 ml of acetic acid and 2.43 g of potassium cyanate and the mixture is stirred at 60° C. for 1 hour. Then, 20 ml of a saturated aqueous solution of sodium hydrogen carbonate and 20 ml of water are added and the mixture is cooled. The resulting crystals are collected by filtration, rinsed and dried to give 2.08 g of 6-(2-carbamoylaminoethylthio)imidazo[1,2-b]pyridazine as colorless crystals melting at 216° to 217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921851 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-22429a8aa05745aba46ab3fe8dbd9063 |
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| Source note | uspto-grants-1990_05 |
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