Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 58016012 | HCID 58016012 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58015762 | HCID 58015762 | — |
Reaction Steps
To a solution of allyl-(5-bromo-2-chloro-pyrimidin-4-yl)-(1-ethyl-propyl)-amine (2.76 g, 8.7 mmol) in anhydrous DMF (15 ml) was added 8 mol % of Pd(OAc)2 (156 mg, 0.69 mmol) and 8 mol % of PPh3 (182 mg, 0.69 mmol) and triethylamine (2.4 ml, 17.3 mmol) a The reaction is stirred at 100° C. overnight. The reaction mixture is diluted with EtOAc, washed with water, dried over Na2SO4, and concentrated in vacuo. Purification with column chromatography (SiO2, 1:2 EtOAC/Hexane) gives the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324225B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-352f115d6cbc45b2826deeebaf10ffec |
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| Source note | uspto-grants-2012_12 |
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