HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797103Generated: October 30, 2026
Triphenylphosphine → HCID 10192636, compound
https://huagongshe.com/reaction/1797103
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Amino-2-bromopyridine | HCID 346455 | — |
| Reactant | HCID 4372073 | HCID 4372073 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10192636 | HCID 10192636 | 39.2% |
Reaction Steps
Under inert atmosphere (Ar) a mixture of palladium-(II)-acetate (0.117 mg, 0.5 mmol) and triphenylphosphine (0.248 g, 0.9 mmol) in DMF (13 ml) was stirred for 30 min at rt. 2-Bromo-pyridin-4-ylamine (0.90 g, 5.2 mmol) (H. J. den Hertog, C. R. Kolder and W. P. Combe, Rec. Trav. Chim., 1951, 70, 591) was added followed by tributyl-styryl-stannane (3.93 g, 10 mmol). After heating at 130° C. for 15 min the solvent was evaporated and the residue partitioned between AcOEt and 3N HCl. The aqueous phase was neutralized with 6N NaOH and extracted with AcOEt. The organic phase was dried with Na2SO4, concentrated and chromatographed (SiO2 with CH2Cl2/CH3OH/NH4OH=140/10/1) to give the title compound (0.40 g, 39%) as a colorless solid. Mp. 164–165° C. (AcOEt), MS: 196 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07034044B2 |
|---|
| Source dataset | uspto-grants-2006_04 |
|---|
| ORD ID | ord-3120aeeadfad4aeb81979b6a17f2063a |
|---|
| Source note | uspto-grants-2006_04 |
|---|