HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dideoxycytidine → Diisopropylaminomethylene 2',3'-dideoxycytidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dideoxycytidine | HCID 24066 | — |
| Reactant | Diisopropylformamide Dimethylacetal (>90%) | HCID 13161384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diisopropylaminomethylene 2',3'-dideoxycytidine | HCID 131717010 | 79.3% |
Reaction Steps
In a typical reaction--previously dried 2',3'-dideoxycytidine (153 mg, 0.724 mmoles) prepared by the literature procedures described above is treated with diisopropylformamide dimethylacetal (1.27 g, 7.24 mmoles) in anhydrous DMF (2 mL) under an argon atmosphere. The contents are stirred overnight and then the solvent and excess reagent are removed by rotary evaporation. The syrupy residue remaining is crystallized from ethanol-ether to give pale lemon-colored crystals (185 mg, 79%) of diisopropylaminomethylene 2',3'-dideoxycytidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05051498 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-fa786e27cfb34f2f97e82278b77890f2 |
| Source note | uspto-grants-1991_09 |