HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributyl(prop-1-yn-1-yl)stannane → HCID 58539200, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributyl(prop-1-yn-1-yl)stannane | HCID 2733165 | — |
| Reactant | HCID 58539140 | HCID 58539140 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58539200 | HCID 58539200 | — |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
A mixture of (4-(5-bromo-4-(methylamino)pyrimidin-2-ylamino)-3-methoxyphenyl)(morpholino)methanone (140 mg, 0.233 mmol), Pd(PPh3)4 (50 mg, 0.04 mmol) and tributyl(prop-1-ynyl)stannane (0.20 mL, 0.66 mmol) in toluene (5 mL) was stirred in a sealed tube at 110° C. for 1 hour. The reaction mixture was filtered and concentrated. Purification of the crude product was achieved by reverse phase HPLC (9 mg, 10%). Additional compounds made using the above procedure are shown in Table 4 above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354420B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-a7d00cf2d42d4d6f9c2c2d01bf170c51 |
| Source note | uspto-grants-2013_01 |