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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508353Generated: October 29, 2026

Isoamyl Nitrite → HCID 25234836, compound

https://huagongshe.com/reaction/508353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 25234760HCID 25234760—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 25234836HCID 2523483648.4%

Reaction Steps

To a solution of the product from Example 83 (30 mg, 0.071 mmol) in anhydrous 1,4-dioxane (3 mL) under N2 was added isoamyl nitrite (19 μL, 0.142 mmol). The resulting mixture was stirred at reflux for 1 h, and concentrated in vacuo. The crude product was purified by C-18 reverse-phase HPLC using an acetonitrile:H2O (0.1% TFA) gradient to give the title compound (14 mg, 48%). 1H NMR (300 MHz, DMSO-d6) δ 11.42 (d, J=1.84 Hz, 1H) 9.44 (s, 1.14) 8.34 (d, J=1.47 Hz, 1H) 8.19 (d, J=8.46 Hz, 1H) 7.79 (d, J=7.72 Hz, 1H) 7.73 (dd, J=8.46, 1.84 Hz, 1H) 7.32-7.37 (m, 2H) 5.65 (dd, J=7.91, 2.39 Hz, 1H) 3.24 (s, 3H) 1.42 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095590B2
Source datasetuspto-grants-2015_08
ORD IDord-fc4d43440a1e403c8a572333285ad6c9
Source noteuspto-grants-2015_08