Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86735642 | HCID 86735642 | — |
| Solvent | Acetyl chloride | HCID 6367 | — |
| Product | HCID 86735641 | HCID 86735641 | — |
Reaction Steps
To a solution of 27g of 3-(2'-hydroxypropyl)methylamino-6-hydrazinopyridazine dihydrochloride in 200 ml of anhydrous pyridine, 7 ml of acetyl chloride are slowly added dropwise at 0° C. When addition is completed, the reaction mixture is left to stand under stirring for two hours at 0°-5° C and then overnight at 0° C. The pyridine is removed by distillation in the rotating evaporator under vacuum at approximately 10° C and an oily residue is obtained which is treated at 0° C and under stirring with a solution of sodium methylate. The product obtained is dried at 10° C, the residue taken up with isopropyl alcohol, filtered on cellite cake and the filtrate, dried under vacuum, gives 3-(2'-hydroxypropyl) methylamino-6-(2'-acetylhydrazino)pyridazine which, recrystallized from ethyl alcohol, melts at 168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04086343 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-2173f33ec5a9449ea9f488ba77121f64 |
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| Source note | uspto-grants-1978_04 |
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