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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037363Generated: November 2, 2026

Sodium Nitrite → HCID 178452585, compound

https://huagongshe.com/reaction/1037363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
Reactant{1-[4-(7,8-diamino-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl esterHCID 67067961—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 178452585HCID 17845258563%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of {1-[4-(7,8-diamino-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester (80 mg, 0.16 mmol) in glacial acetic acid (2 mL) and water (1 mL) at 0° C. was added NaNO2 (14 mg, 0.20 mmol). The resulting mixture was stirred at 0° C. for 30 mins, before allowing to warm to RT. After 16 hours, further NaNO2 (14 mg, 0.20 mmol) was added and the reaction mixture stirred at RT for a further 3 hours. The resultant mixture was poured onto water and the aqueous mixture was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with NaHCO3 (2×30 mL), brine, dried (NaSO4), filtered, and the solvent removed in vacuo to give the title compound as a brown solid (51 mg, 63%). LCMS (Method G): RT=3.76 min, [M+H]+=509.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-6ef124e2abfd4178996074d063e5e19f
Source noteuspto-grants-2013_10