HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 11712708, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Prolinol, (R)- | HCID 2724541 | — |
| Reactant | Ethanol, 2-[[4-[[3-fluoro-4-[(6-methyl-3-pyridinyl)oxy]phenyl]amino]-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy]-, 1-methanesulfonate | HCID 11719830 | — |
| Product | HCID 11712708 | HCID 11712708 | 30% |
Reaction Steps
The procedure described in Example 23 was repeated (except that potassium iodide was not used) using 2-{[4-({3-fluoro-4-[(6-methylpyridin-3-yl)oxy]phenyl}amino)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]oxy}ethyl methanesulfonate (prepared as described in Example 20) and (R)-2-pyrrolidinemethanol to give the title compound in 30% yield; NMR Spectrum: 1.51 (m, 1H), 1.65 (m, 2H), 1.80 (m, 1H), 2.33 (q, 1H), 2.45 (s, 3H), 2.57 (m, 1H), 2.78 (dt, 1H), 3.14 (t, 1H), 3.28 (hidden by DMSO, 2H), 4.41 (t, 2H), 4.47 (br s, 1H), 7.25 (m, 3H), 7.56 (d, 1H), 7.85 (td, 1H), 8.01 (dd, 1H), 8.24 (d, 1H), 8.37 (s, 1H), 8.59 (br s, 1H); Mass Spectrum: 480 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947676B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-157801aa54e64688b3c25ba845574cdf |
| Source note | uspto-grants-2011_05 |