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HRID 395716作成日:2026年10月25日

P-Anisidine → 2-(4-Tert-butylbenzoylamino)-5-nitro-n-(4-methoxyphenyl)benzamide

https://huagongshe.com/reaction/395716

反応式

関与物質

役割名称HCID仕込み量
反応物P-AnisidineHCID 7732—
反応物2-(4-Tert-butylphenyl)-6-nitro-3,1-benzoxazin-4-oneHCID 385599—
溶媒DimethylformamideHCID 6228—
生成物2-(4-Tert-butylbenzoylamino)-5-nitro-n-(4-methoxyphenyl)benzamideHCID 1067109914.5%

反応条件

温度80 °C

反応手順

A mixture of 6-nitro-2-(4-tert-butylphenyl)-4H-3,1-benzoxazin-4-one (1.21 g, 3.73 mmol) and p-anisidine (551 mg, 4.47 mmol) in N,N-dimethylformamide (5 mL) was heated at 80° C. for 2.5 h. After cooling to room temperature, the reaction mixture was poured into an ice/water mixture and extracted twice with methylene chloride. The combined organic layers were washed with water, dried (sodium sulfate), and filtered. From the resulting solution crystallized 706 mg (42%) of the title product as a light brown solid. The mother liquor was chromatographed (silica gel, 20% diethyl ether/80% hexanes to 40% diethyl ether/60% hexanes) to give 242 mg (14%) of additional product; mp 210-11° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-2122cdd1c1bd490d902598d7cf226088
出典メモuspto-grants-2003_08