HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 59239140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59239135 | HCID 59239135 | — |
| Reactant | HCID 59239154 | HCID 59239154 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59239140 | HCID 59239140 | 100% |
Reaction Steps
Step 1—Synthesis of (S)-6-(benzyloxy)-N-(4-(7-methyl-4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)pyridin-2-amine (mt): (S)-6-(benzyloxy)-N-(4-(4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)pyridin-2-amine (ms) (100 mg, 0.2 mmol) was dissolved in DMF (2 mL) and DIPEA (159 μL, 0.9 mmol)). To this solution was added MeI (14 μL, 0.2 mmol) at rt. The resulting solution was stirred at rt for 4 hrs. It was diluted with H2O, extracted with EtOAc (2×10 mL). The combined organics were washed with brine, dried over Magnesium sulfate, filtered, concentrated in vacuo to afford 100 mg (100%) of the title compound mt. LC-MS: m/z=+524 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163763B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-018def37e6a04a619b1a77d0958f053b |
| Source note | uspto-grants-2012_04 |