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HRID 1168532作成日:2026年10月27日

1-Boc-1-methylhydrazine → ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoate

https://huagongshe.com/reaction/1168532

反応式

関与物質

役割名称HCID仕込み量
反応物1-Boc-1-methylhydrazineHCID 3748280—
反応物Ethyl 2-(2,3-Difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoateHCID 69879816—
溶媒tert-ButanolHCID 6386—
生成物ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-[2-methyl-2-[(2-methylpropan-2-yl)oxycarbonyl]hydrazinyl]prop-2-enoateHCID 17847213992.2%

反応手順

A solution of ethyl 2-(2,3-difluoro-5-iodobenzoyl)-3-ethoxy-2-propenoate (Preparation 21, 7.80 g) in tert-butanol (40 mL) is cooled with a cold water bath and a solution of tert-butyl 1-methylhydrazinecarboxylate (2.92 g) in tert-butanol (4 mL) is added. The cooling bath is removed, the mixture is stirred for 5 min at ambient temperature, and then is heated in an oil bath at 45° C. for 40 min. The reaction mixture is poured into 100 mL of crushed ice/water and extracted two times with ethyl acetate. The combined organic layers are dried (Na2SO4) and concentrated in vacuo. The crude product is purified by chromatography, using 300 g of silica gel, packed and eluted with EtOAc/heptane (1/3), to afford 8.95 g (92%) of the title compound as a yellow oily foam. Physical characteristics: 1H NMR (CDCl3) δ8.14, 8.07, 7.59-7.49, 7.46-7.41, 4.07, 3.30, 3.26, 1.50, 1.09, 0.97; MS (ESI+) m/z 511 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06624159B2
出典データセットuspto-grants-2003_09
ORD IDord-64a0e742feee401781161d683297aaa4
出典メモuspto-grants-2003_09