HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10632308, compound → HCID 20716774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10632308 | HCID 10632308 | — |
| Reactant | HCID 20716771 | HCID 20716771 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20716774 | HCID 20716774 | 98% |
Reaction Steps
To a solution of 2′-O-(5-aminopentyl)-5′-O-(4,4′-dimethoxytrityl)-adenosine (1.0 g, 1.52 mmol) in anhydrous CH3CN (8.0 mL) was added with stirring, under argon, N-(2-Cyanoethoxycarbonyl)oxy succinimide (0.43 g, 2.02 mmol) After stirring for 5 h at room temperature the reaction mixture was diluted with EtOAc (50 mL) and washed with aq saturated bicarbonate (3×20 mL) and water (20 mL), dried (Na2SO4) and evaporated to give 53 as a light yellow foam (1.1 g, 98% yield). This compound was used without further purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861514B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-e007eeea0fdc48698d69efc11c8b2b04 |
| Source note | uspto-grants-2005_03 |