戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 81559作成日:2026年10月26日

Ammonia → (R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

https://huagongshe.com/reaction/81559

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物tert-Butyl hydroperoxideHCID 6410—
反応物Sodium ThiosulfateHCID 24477—
反応物Ammonia hydroxideHCID 21862953—
反応物(R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thioneHCID 86667520—
溶媒MethanolHCID 887—
生成物(R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamineHCID 86716531—

反応手順

(R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thione (2.86 g, 7.77 mmol) was dissolved in 7M NH3 in methanol (50 ml). Tert-Butylhydroperoxide (9.41 ml, 78 mmol) and ammonia hydroxide (25% sol., 21.2 ml, 136 mmol) were added and the reaction was stirred at r.t. for 2 hrs. Upon completion, 50 ml half-saturated Na2S2O3 solution was added to the reaction and the product was extracted with ethyl acetate. The organic phases were washed with water and brine, combined and dried over Na2SO4. Volatiles were removed under reduced pressure, yielding the title compound as yellowish solid. 1H-NMR (360 MHz, DMSO-d6): 8.34 (s, 1H), 8.25 (s, 1H), 8.12 (s, 1H), 5.85 (br, 2H), 4.01 (m, 1H), 3.80 (m, 1H), 3.55 (m, 1H), 1.38 (s, 3H); MS: 314 [(M+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846658B2
出典データセットuspto-grants-2014_09
ORD IDord-adb68345b7214d86b2eae8950c5ec4b1
出典メモuspto-grants-2014_09