HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657855Generated: November 1, 2026
Cyanogen Bromide → HCID 58045867, compound
https://huagongshe.com/reaction/657855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-hydrazinyl-6-(1H-imidazol-1-yl)pyridazine | HCID 3031323 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58045867 | HCID 58045867 | 11.6% |
Reaction Steps
(6-Imidazol-1-ylpyridazin-3-yl)hydrazine (500 mg) were initially charged in a mixture of acetic acid (4 ml) and water (8 ml) with addition of sodium acetate (232 mg) at RT while stirring. Thereafter, the mixture was cooled to 0° C. and cyanogen bromide (330 mg) was introduced in portions. After stirring for 2.5 h, the mixture was left to stand overnight. After cooling to 0° C., the mixture was alkalized with 10 M sodium hydroxide solution and extracted repeatedly with EA. The combined EA phases were dried over sodium sulfate, filtered and concentrated. 66 mg of the title compound were isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076336B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5a036a86ac02487da2fa37c559008312 |
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| Source note | uspto-grants-2011_12 |
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