Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178513358 | HCID 178513358 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 59484918 | HCID 59484918 | — |
Reaction Steps
2.8 ml of glacial acetic acid, 2.3 ml of acetic anhydride and 200 μl of pyridine are added to 375 mg (2.43 mmol) of N-hydroxy-6-oxo-1,6-dihydropyridazine-3-carboxamidine, and the mixture is stirred at 90° C. for 15 h. During cooling of the reaction mixture, a precipitate forms, which is filtered off with suction, washed with water and dried in vacuo; yield: 253 mg, yellow solid; HPLC: Rt=1.51 min; LC-MS: 179 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921357B2 |
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| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-66409b950abe4217a25628a5b0251fdf |
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| Source note | uspto-grants-2014_12 |
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