Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86760968 | HCID 86760968 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9950702 | HCID 9950702 | 80% |
Reaction Steps
To a solution of 5-(4-carboxy-1,3-butadienyl)-2′-deoxyuridine (VI) (0.200 g, 0.62 mmol) in DMF (1 mL) was added KHCO3 (0.185 g, 1.84 mmol) and the mixture was stirred for 20 mm at 25° C. A solution of N-bromosuccinimide (0.117 g, 0.65 mmol) in DMF (0.3 mL) was added dropwise. Smooth gas evolution (CO2) occurred throughout the addition. The resulting brown suspension was stirred for 2 h at 25° C. at which time TLC showed that (VI) was completely consumed. Water (10 mL) was added to the suspension and the resulting solution was extracted with EtOAc (2×15 mL). The extract was dried over MgSO4 and the solvent was evaporated in vacuc to give a yellow solid (178 mg, 80% yield) consisting of a mixture of two isomers as shown by 1H NMR. The crude product was separated by semi-preparative HPLC (reversed phase C18 column) using 20% acetonitrile in water as the mobile phase to give the following isomers:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07605144B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-0f226139f23e481ab5d5e9ff263217ef |
|---|
| Source note | uspto-grants-2009_10 |
|---|