HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adenosine → HCID 135412808, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adenosine | HCID 60961 | — |
| Reactant | HCID 15450639 | HCID 15450639 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 135412808 | HCID 135412808 | 48% |
Reaction Steps
114 mg of the crude anomer mixture of 9-(2-deoxy-2-fluoro-4-thio-D-arabinofuranosyl)-2,6-diaminopurine (beta/alpha=1.55) obtained in Synthesis Example 2 was suspended in 25 ml of tris hydrochloric acid buffer solution (pH=7.0). To this suspension was added 0.43 ml (100 units) of adenosine deaminase, and the mixture was stirred at room temperature for 6 hours. The reaction solution was purified by ODS reverse phase column chromatography to obtain 48 mg (yield 48%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06103707 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-ae6abeed2d9c498292316fead190f678 |
| Source note | uspto-grants-2000_08 |