HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512864Generated: October 27, 2026
Diisopropylethylamine → 6-fluoro-1-(1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-yl)-1H-indazole
https://huagongshe.com/reaction/512864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-fluoro-1-(piperidin-4-yl)-1H-indazole | HCID 53923964 | — |
| Reactant | 3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine | HCID 54595607 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-fluoro-1-(1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-yl)-1H-indazole | HCID 76311098 | — |
Reaction Steps
6-Fluoro-1-(piperidin-4-yl)-1H-indazole (260 mg, 1.19 mmol), 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyridazine (230 mg, 1.19 mmol) and DIEA (269 uL) in DMSO (4 ml) under Ar were heated in a microwave reactor at 200° C. for 1 hour. After removal of most of the DMSO in vacuo, water (10 mL) was added and the aqueous layer extracted several times with CHCl3 (50 mL). The organic layer was washed with brine, dried (MgSO4), decolorized with NORITE, filtered and the solvent removed in vacuo. The resulting residue was purified via ISCO column chromatography (Amine “Redisep” 14 gram column eluded 0-100% EtOAc/hexane over 20 column volumes), then re-crystallized from DCM with heptanes to yield 6-fluoro-1-(1-(6-(1-methyl-1H-pyrazol-4-yl)pyridazin-3-yl)piperidin-4-yl)-1H-indazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102669B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-8875cd278f3a47ff88de0577b4d32e7d |
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| Source note | uspto-grants-2015_08 |
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