HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79263Generated: October 28, 2026
Potassium Phosphate, Tribasic → 1-benzyl-3-cyclopropyl-4-nitro-1H-indazole
https://huagongshe.com/reaction/79263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | HCID 67261440 | HCID 67261440 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-benzyl-3-cyclopropyl-4-nitro-1H-indazole | HCID 67260039 | 68.5% |
Reaction Steps
To a reaction vial was added 1-benzyl-3-bromo-4-nitro-1H-indazole (100 mg, 0.301 mmol), cyclopropylboronic acid (33.6 mg, 0.391 mmol) and potassium phosphate (192 mg, 0.903 mmol). Toluene (1.5 mL) and water (0.1 mL) were added. The mixture was purged with argon for 30 minutes. Palladium (II) acetate (3.38 mg, 0.0151 mmol) and tri-cyclohexyl phosphine (8.44 mg, 0.0301 mmol) were added. The reaction vessel was purged with argon and sealed. The mixture was heated at 100° C. for 24 hours. The mixture was filtered through glass fiber filter paper, washing with ethyl acetate and methanol followed by concentration under reduced pressure. The material was purified by preparative chromatography on silica, eluting with hexane/ethyl acetate (5:1). The band containing the desired product was isolated and concentrated under reduced pressure to give 1-benzyl-3-cyclopropyl-4-nitro-1H-indazole (60.5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841455B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-50a3a9c0ac97412c823cb26c28565544 |
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| Source note | uspto-grants-2014_09 |
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