HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334463Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 178434440, compound
https://huagongshe.com/reaction/334463
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 3-Acetyl-2-chloropyridine | HCID 10942697 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178434440 | HCID 178434440 | — |
Reaction Steps
To a solution of the above crude 1-(2-chloropyridin-3-yl)ethanone (XIII) in n-BuOH (512 L) was added 85% hydrazine hydrate (78 L, 1360 mol). The reaction was heated at refluxed (˜120° C.) for 48 hours. The reaction was cooled and evaporated under vacuum. The crude material was taken up in DCM (834 L) and washed with 2× aqueous 25% NaCl (214 L) by adding aqueous 25% NaCl, stirring for 50 min, allowing to stand for 50 min, separating the layers and then repeating. The organic layer was evaporated to produce 3-methyl-1H-pyrazolo[3,4-b]pyridine (XIV) as a solid (13.2 Kg, 99 mol, 94.1% purity, 36.3% assay yield for 3 steps). 1H NMR (DMSO-d6, 400 MHz) δ ppm 2.50 (s, 3H), 7.13 (dd, J=4.4 Hz, J=8 Hz, 1H), 8.19 (dd, J=1.2 Hz, J=8 Hz, 1H), 8.47 (dd, J=1.6 Hz, J=4.8 Hz, 1H), 13.18 (brs, 1H); ESIMS found C7H7N3 m/z 133.8 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883822B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-e10f5bf6b1d448ce92fc5dcd7324efa8 |
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| Source note | uspto-grants-2014_11 |
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