HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Nitrite → HCID 86612908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 86612909 | HCID 86612909 | — |
| Catalyst | Tetraethylammonium Bromide | HCID 6285 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86612908 | HCID 86612908 | 80% |
Reaction Steps
To a solution 4-amino-2-(2-C-methyl-β-D-ribofuranosyl)-2,6-dihydro-7H-2,3,5,6-tetraazabenzo[cd]azulene-7-one 15.6 (35 mg, 0.1 mmol) in 50% aqueous acetic acid (5 mL) was added sodium nitrite (42 mg, 0.6 mmol) and the mixture stirred at room temperature for 4 hr. The mixture was neutralized with 1M TEAB buffer and purified by reversed phase ion-pairing HPLC on a Phenomenex Luna C18(2) 250×21 mm 10 μM column. 100 mM triethylammonium acetate (TEAA), pH 7 was used as the ion-pairing agent. A gradient of 20% to 55% MeOH over 40 min was applied. The target compound eluted at 26 min followed by two smaller peaks at 29 and 31 min. TEAA was removed by repeated lyophilzation to yield the target compound as a fluffy yellow material (28 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713941B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-748460beece24d7093865d55a4056375 |
| Source note | uspto-grants-2010_05 |