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HRID 589059作成日:2026年10月25日

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

https://huagongshe.com/reaction/589059

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene--cyclohexane (1/1)HCID 18624872—
反応物5-nitro-3-pyridin-2-yl-2H-1,4-benzoxazineHCID 90408902—
反応物HCID 178506846HCID 178506846—
溶媒TetrahydrofuranHCID 8028—
生成物3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazineHCID 90409367—

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227985B2
出典データセットuspto-grants-2016_01
ORD IDord-201ae97b463f4655806c488d4a39f5b9
出典メモuspto-grants-2016_01