HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73Generated: October 23, 2026
4-Aminobenzonitrile → HCID 178418220, compound
https://huagongshe.com/en/reaction/73
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 6-chloro-N-cyclohexylpyridine-3-carboxamide | HCID 857493 | — |
| Reagent | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178418220 | HCID 178418220 | 9.93% |
Reaction Steps
In a 50 mL round-bottomed flask a TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.115 g, 0.13 mmol),POTASSIUM TERT-BUTOXIDE (0.282 g, 2.51 mmol)and BINAP (0.157 g, 0.25 mmol) in dry 1,4-dioxane (10 mL) was mixed under N2.Followed by 6-chloro-N-cyclohexylnicotinamide (.300 g, 1.26 mmol) and 4-aminobenzonitrile (0.178 g, 1.51 mmol) was added and resulting mixture(dark brown) was heated at 100oC for 3 hrs.LCMS analysis showed the formation of required product.Reaction stopped,crude was passed through celite and washed with dioxane and finally with methanol.The filtrate was dried and dissolved in 3 ml DMSO for Waters MS Purification system.Pure fractions collected and concentrated.A White solid obtained as a product 6-(4-cyanophenylamino)-N-cyclohexylnicotinamide (0.040 g, 9.93 %).32 mg of above product was submitted for MGyrx2 projetct.LCMS/NMR confirmed the product.
Provenance & Evidence
| Source dataset | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-2d4104aef43247ff855d465ce3910528 |
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| Source note | 750 AstraZeneca ELN dataset |
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