Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Acryloylmorpholine | HCID 98723 | — |
| Reactant | HCID 22137416 | HCID 22137416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69591888 | HCID 69591888 | — |
Reaction Steps
To a solution of (4-iodo-phenyl)-[4-(tetrahydro-pyran-2-yloxy)-benzyl]-amine (0.265 g, 0.65 mmol) in 2 mL dimethylformamide was added 4-acryloylmorpholine (0.110 g, 0.78 mmol), Pd(OAc)2 (0.029 g, 0.13 mmol), and triethylamine (0.20 mL, 1.43 mmol). The reaction was stirred at 90° C. for 2 hr. Triphenylphosphine (0.101 g, 0.38 mmol) and additional Pd(OAc)2 (0.032 g, 0.14 mmol) were added and the reaction mixture was stirred at 90–100° C. for 18 hr. The reaction mixture was cooled, water was added, and the aqueous solution was washed ethyl acetate (3×). The combined organic layers were dried (magnesium sulfate) and concentrated. Medium pressure silica gel chromatography (33% ethyl acetate/hexanes to 50% ethyl acetate/hexanes) afforded the title compound of Step A. MS 423.0 (M+1)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053212B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-829896c40fae42c2899c24dff3e2714c |
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| Source note | uspto-grants-2006_05 |
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