HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adenosine → HCID 136205272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adenosine | HCID 60961 | — |
| Reactant | HCID 15858693 | HCID 15858693 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Trisodium Phosphate | HCID 24243 | — |
| Product | HCID 136205272 | HCID 136205272 | — |
Reaction Steps
2,6-diamino-9-(2-O-pentyl-β-D-ribofuranosyl)purine (1.9 g) in 0.1 M sodium phosphate buffer (50 ml, pH 6.0) and DMSO (25 ml) was treated with adenosine deaminase (added in two aliquots—first aliquot 50 mg, second aliquot 80 mg) at 35° C. as per the procedure of Example 3 to yield 1.4 g of product. 1H NMR (DMSO-d6) δ 0.8 (t, 3, CH3), 1.16 (m, 4, 2×CH2), 1.4 (m, 2, CH2), 3.38, 3.6 (m, 4, OCH2, H-5′), 3.93 (s, 1, H-4′), 4.28 (m, 2, H-2′, H-3′), 5.17 (br, 2, 5′, 3′-OH), 5.8 (d, 1, H-1′), 6.53 (br s, 2, NH2), 8.0 (s, 1, H-8) and 10.68 (br, 1, NH)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101993B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-3d112704df714d8c93f4a0b3a6c55721 |
| Source note | uspto-grants-2006_09 |