HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42202Generated: October 25, 2026
2-(Dicyclohexylphosphino)biphenyl → HCID 59240555, compound
https://huagongshe.com/reaction/42202
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Reactant | 1-Benzyl-4-piperazin-1-yl-phthalazine | HCID 6404023 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-(6-Chloro-pyridin-3-yl)-1-pyrrolidin-1-yl-ethanone | HCID 57471614 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59240555 | HCID 59240555 | — |
Reaction Steps
To a solution of this amide (0.22 g, 1 mmol) and 1-benzyl-4-piperazin-1-yl-phthalazine (0.15 g, 0.5 mmol) in toluene (10 mL) were added (2-biphenyl)dicyclohexyl phosphine (35 mg, 0.1 mmol), Pd(OAc)2 (11 mg, 0.05 mmol) and KOtBu (336 mg, 3 mmol). The mixture was degassed and then heated in a microwave reactor at 90° C. The reaction mixture was cooled to room temperature and filtered. Water was added to the filtrate and extracted with EtOAc. The combined organic layers were washed with water, sat. NaHCO3, brine, dried over Na2SO4, filtered and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536168B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-3d0271881ab04280b77fec1a26ed43cb |
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| Source note | uspto-grants-2013_09 |
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