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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 589059Erstellt: 24. Oktober 2026

Benzene--cyclohexane (1/1) → 3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/de/reaction/589059

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene--cyclohexane (1/1)HCID 18624872—
Edukt5-nitro-3-pyridin-2-yl-2H-1,4-benzoxazineHCID 90408902—
EduktHCID 178506846HCID 178506846—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazineHCID 90409367—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

0.5 M Ethyl lithium in benzene-cyclohexane (1.8 mL, 0.88 mmol) was added drop-wise to a solution of 5-nitro-3-pyridin-2-yl-2H-1,4-benzoxazine (0.025 g, 0.88 mmol) in tetrahydrofuran (4 mL), cooled to −78° C. The reaction was stirred for 1 h at −78° C. and was then quenched with methanol. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated to give crude product. The product was purified by FCC on silica gel eluting a hexane:ethyl acetate gradient to give 3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazine as a solid (0.021 g. 84%). LCMS calculated for C15H16N3O3 (M+H)+: m/z=286.1. found: 286.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09227985B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-201ae97b463f4655806c488d4a39f5b9
Quellennotizuspto-grants-2016_01