HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972715Generated: October 26, 2026
Hydrazine hydrate (1:1) → 6-chloro-5-fluoro-1H-indazole
https://huagongshe.com/reaction/1972715
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Chloro-2,5-difluorobenzaldehyde | HCID 18991142 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 6-chloro-5-fluoro-1H-indazole | HCID 58529904 | 16% |
Reaction Steps
A mixture of 4-chloro-2,5-difluorobenzaldehyde (20.6 g, 105.0 mmol) and hydrazine hydrate (77.2 mL, 1575.2 mmol, 15 eq) in n-butanol (35 mL) was stirred at 140° C. for 3 days. The mixture was cooled to room temperature and poured into ice water (750 mL). The mixture was stirred vigorously for 2 h, and the orange solid was filtered. The filtrate was extracted with EtOAc (3×250 mL), and the combined organic phases were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was combined with the orange solid and then purified by MPLC (Biotage®, gradient elution 25% EtOAc/hexane) to give 2.81 g (16%) of a white solid. 1H-NMR (300 MHz, DMSO-d6) 13.3 (broad s, 1H), 8.09 (s, 1H), 7.80 to 7.76 (m, 2H); ES-MS m/z 171.2/173.2 [M+H]+, RT (min) 3.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-ca8e8fec3bcc494cb61974422831e457 |
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| Source note | uspto-grants-2013_04 |
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