HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401464Generated: October 29, 2026
Methylhydrazine → HCID 67197081, compound
https://huagongshe.com/reaction/401464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 86670587 | HCID 86670587 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67197081 | HCID 67197081 | 68% |
Reaction Steps
To a solution of 6-(pyridin-3-yl)imidazo[1,2-a]pyridine-3-carbaldehyde (Intermediate 1, 70 mg, 0.31 mmol) in ethanol (3 mL) was added methyl hydrazine (17 mg, 0.47 mmol) at RT. The reaction was heated at 85° C. for 3 h. Ethanol was evaporated. Pyridine (2 mL) was added to this residue, followed by addition of benzene sulfonylchloride (83 mg, 0.47 mmol). The reaction mixture was stirred at RT overnight. Pyridine was evaporated. Water was added to this residue and extracted with dichloromethane. Organic layer was dried over sodium sulfate and evaporated. The crude product was purified by column chromatography (silica gel, 1.5% methanol in chloroform) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741932B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-fab4bf0c9e2043fa89dbd65dc8dc27b8 |
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| Source note | uspto-grants-2014_06 |
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