HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → (S)-2-(2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidin-7(8H)-yl)-N,N-dimethylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-chloro-N,N-dimethylacetamide | HCID 75886 | — |
| Reactant | Urea, N-ethyl-N'-[4-[5,6,7,8-tetrahydro-4-[(3S)-3-Methyl-4-Morpholinyl]pyrido[3,4-d]pyriMidin-2-yl]phenyl]- | HCID 46913570 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-2-(2-(4-(3-ethylureido)phenyl)-4-(3-methylmorpholino)-5,6-dihydropyrido[3,4-d]pyrimidin-7(8H)-yl)-N,N-dimethylacetamide | HCID 59239517 | — |
Reaction Steps
(S)-1-ethyl-3-(4-(4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)urea (0.086 mmol), N,N-diisopropylaethylamine (0.26 mmol), potassium iodide (0.06 mmol) were mixed in DMF (0.4 mL), then 2-chloro-N,N-dimethylacetamide was added. The mixture was stirred at room temperature for ˜3 h and the product was purified by reverse-phase HPLC to give the desired product. LC-MS: m/z=+482 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163763B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c903939e62d546ef916d8ba234804d50 |
| Source note | uspto-grants-2012_04 |