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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234799Generated: October 30, 2026

Sodium Nitrite → HCID 86612908, compound

https://huagongshe.com/reaction/2234799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86612909HCID 86612909—
CatalystTetraethylammonium BromideHCID 6285—
SolventAcetic AcidHCID 176—
ProductHCID 86612908HCID 8661290880%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713941B2
Source datasetuspto-grants-2010_05
ORD IDord-748460beece24d7093865d55a4056375
Source noteuspto-grants-2010_05