HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529377Generated: November 4, 2026
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole
https://huagongshe.com/reaction/1529377
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Dicyclohexyl(2',4',6'-tripropyl-[1,1'-biphenyl]-2-yl)phosphine | HCID 21081571 | — |
| Reactant | 3-(6-chloropyrazin-2-yl)-5-(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole | HCID 86709779 | — |
| Reactant | HCID 178419765 | HCID 178419765 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole | HCID 67959807 | 21.4% |
Reaction Steps
A microwave tube was charged with 3-(6-chloropyrazin-2-yl)-5-(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (Ex. 243e, 111 mg, 0.256 mmol), Pd(OAc)2 (3 mg, 0.013 mmol) and 2-(dicyclohexylphosphino)-2′,4′,6′-tri-1-propyl-1,1′-biphenyl, (X-Phos) (12 mg, 0.026 mmol) and the tube was sealed. The tube was evacuated under vacuum and backfilled with N2 (3×). THF (1.7 mL) was added and the mixture was cooled in an ice-water bath. Cyclopropylzinc bromide solution (0.5 M in THF, 0.62 mL, 0.31 mmol, Sigma-Aldrich) was added and the mixture was warmed to RT and stirred for 2 h. The mixture was filtered and the crude was purified by silica gel chromatography, eluting with a gradient of 0-50% EtOAc in hexanes, to provide 24 mg of 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole. The column was eluted with 2-10% MeOH in CH2Cl2 to afford 50 mg of 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole. The two portions were combined to give 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (74 mg, 0.17 mmol, 66% yield) as a yellow foam. MS (ESI, pos. ion) m/z: 439.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-5e1b1eaf95b5493e846b93d3763c86f0 |
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| Source note | uspto-grants-2015_07 |
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