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HRID 484408作成日:2026年10月26日

Benzoyl Peroxide → N-[(7-bromo-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide

https://huagongshe.com/reaction/484408

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物N-[(9,9a-Dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamideHCID 19795217—
溶媒AcetonitrileHCID 6342—
生成物N-[(7-bromo-9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamideHCID 19795216—

反応手順

(±) (1S,9aS/1R,9aR) N-[(9,9a-Dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide (X, diastereomer B, [SS,RR-trans], EXAMPLE 11, 299 mg) is dissolved in acetonitrile (10 ml). To this mixture N-bromosuccinimide (235 mg) and a catalytic amount of benzoylperoxide are added as solids to the mixture at 20°-25°. The mixture is stirred at 20°-25° in a sealed flask over night. Then a small portion is removed and examined by NMR. The mixture was then concentrated under reduced pressure to give the title compound, NMR (CDCl3, 300 MHz) 7.30, 6.49, 4.63, 4.52, 3.72, 3.29, 3.12, 2.76 and 2.06 δ.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05231188
出典データセットuspto-grants-1993_07
ORD IDord-4bc773dde9e146788712b4858ff30a6d
出典メモuspto-grants-1993_07