Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Trimethylboroxine | HCID 574072 | — |
| Reactant | HCID 57519194 | HCID 57519194 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59333980 | HCID 59333980 | — |
Reaction Steps
To a pressure vessel was added 3-(2-Chloro-5-fluoro-pyrimidin-4-ylamino)-6,6-dimethyl-4,6-dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxylic acid tert-butyl ester (1.50 g, 3.90 mmol), trimethylboroxine (10.9 mL, 78.4 mmol), cesium carbonate (25.5 g, 78.4 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.480 g, 0.588 mmol), H2O (6 mL), and THF (60 mL). The suspension was purged with argon for 2 min, then heat at 100° C. for 15 h. The cooled solution was filtered to remove undissolved solids. Purification by silica gel column chromatography using 0-10% ammoniated methanol in CH2Cl2 provided the desired product H1(i) as a brown solid (0.80 g, 56%). 1H NMR (300 MHz, DMSO-d6) δ ppm 1.41 (s, 9H) 1.57 (s, 6H) 2.38 (s, 3H) 4.43-4.58 (m, 2H) 8.12 (s, 1H) 10.02 (s, 1H) 12.34 (s, 1H). Mass Spectrum: Calcd for C17H24N6O2F (M+H): 363. Found: 363.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877761B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-61f5cc5879a84adea78c040cca5ed273 |
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| Source note | uspto-grants-2014_11 |
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