Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2'-Deoxy-2'-fluoro-2'-methyluridine | HCID 11311503 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66802642 | HCID 66802642 | 94% |
Reaction Steps
Chiral 1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-hydroxymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione (6.14 g, 23.6 mmol), PPh3 (9 g, 34.4 mmol), imidazole (2.4 g, 34.4 mmol) and dry THF (100 mL) were added into a 3-neck flask bottle (500 mL), the mixture was stirred at 20° C. under nitrogen atmosphere for 20 min. Then I2 (6.6 g, 26 mmol) dissolved in dry THF (100 mL) was added into the mixture dropwise at 20° C. during 30 min, after addition, the whole mixture was stirred at 20° C. under nitrogen atmosphere for 18 hrs. TLC showed that the SM was consumed, then water (50 mL) was added into it, the mixture was extracted by EA (150 mL×3), organic layer was washed with brine, dried over Na2SO4, removed solvent by reduced pressure, residue was purified by silica gel chromatography column (DCM:MeOH=100:1 to 50:1) to afford the title compound as a white solid (8.2 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09108999B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-3195089ff26a44eb95669b754bd2de8d |
|---|
| Source note | uspto-grants-2015_08 |
|---|