HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → (S)-1-cyclopropyl-3-(4-(4-(3-methylmorpholino)-6-neopentyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-Cyclopropyl-N'-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea | HCID 44119149 | — |
| Reactant | (S)-4-(2-chloro-6-neopentyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)-3-methylmorpholine | HCID 86663152 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | CPME EtOH Water | HCID 131731673 | — |
| Product | (S)-1-cyclopropyl-3-(4-(4-(3-methylmorpholino)-6-neopentyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)urea | HCID 46912284 | 18.4% |
Reaction Steps
(S)-4-(2-chloro-6-neopentyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)-3-methylmorpholine (intermediate 7) (assumed 0.56 mmol) was stirred in CPME:EtOH:Water (7:3:2, freshly mixed, 2 mL) with 1-cyclopropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea (203 mg, 0.67 mmol), Pd(PPh3)2Cl2 (20 mg, 0.028 mmol) and Na2CO3 (89 mg, 0.84 mmol) under a stream of nitrogen for 5 min, then irradiated in the microwave at 130° C. for 30 min. The reaction mixture was diluted with water and EtOAc and passed through a celite cartridge. The organic layer was concentrated in vacuo and purified by prep HPLC to give the desired compound as a yellow solid (48 mg, 0.103 mmol, 18% yield over three steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785457B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-d7e87a0db2664df294f91efa8687efa1 |
| Source note | uspto-grants-2014_07 |