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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177629Generated: October 30, 2026

Isoamyl Nitrite → HCID 90408508, compound

https://huagongshe.com/reaction/2177629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantTetrafluoroboric acidHCID 28118—
ReactantHCID 90408828HCID 90408828—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 90408508HCID 9040850848%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a slurry of N-(2-chloro-6-methyl-3-nitropyridin-4-yl)-5-fluoropyrimidin-2-amine (13 g, 45.8 mmol) in ethanol (300 mL) was added 10% Pd/C (100 mg). The reaction was stirred for 10 h under a hydrogen atmosphere after which time the reaction was filtered and the filtrate was concentrated. The residue was diluted with ethanol (200 mL) and cooled to 0° C. Isoamyl nitrite (4.0 g, 34.0 mmol) and HBF4 (5.5 g, 34.0 mmol) were added and the reaction was stirred for 30 min at 0° C. followed by rt for 10 h. Evaporation of the solvents followed by recrystallization afforded the product as a white solid (3.2 g, 48%). MS (ESI) mass calcd. C10H7FN6, 230.07. m/z found, 231.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 9.44 (s, 1H), 9.17 (s, 2H), 8.14 (s, 1H), 2.70 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066946B2
Source datasetuspto-grants-2015_06
ORD IDord-d033aa049f384275b76f45d8287601ec
Source noteuspto-grants-2015_06