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HRID 1024431作成日:2026年10月27日

Ammonium Chloride → Methyl 2-(5-(4-aminophenyl)thiazole-2-carboxamido)-3-methylbutanoate

https://huagongshe.com/reaction/1024431

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Methyl 3-methyl-2-(5-(4-nitrophenyl)thiazole-2-carboxamido)butanoateHCID 67150324—
触媒IronHCID 23925—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(5-(4-aminophenyl)thiazole-2-carboxamido)-3-methylbutanoateHCID 6715032992.3%

反応条件

温度80 °C

反応手順

Ammonium chloride (1.04 g) and iron (777 mg) were added to a solution of Methyl 3-methyl-2-(5-(4-nitrophenyl)thiazole-2-carboxamido)butanoate (Intermediate 2, step C, 2.15 g) in EtOH (21.5 ml), THF (8.6 ml), and Water (8.6 ml). The reaction mixture was refluxed at 80° C. for 3 hours. It was then cooled, filtered through celite and the solvent was removed under reduced pressure to get dark brown residue. The residue was taken in water and extracted with ethyl acetate. The organic layer was separated, dried over Na2SO4 and concentrated to get dark brown residue which was purified by column on silica gel in 2.5:7.5 EtOAc:chloroform to get yellow sticky solid which was crystallized in DCM/pet ether to yield 1.82 g (91%) of the title compound. 1HNMR (DMSO-d6, 300 MHz): δ 8.59 (d, 1H), 8.15 (s, 1H), 7.42 (d, 2H), 6.63 (d, 2H), 5.76 (bs, 2H), 4.31 (m, 1H), 3.67 (s, 3H), 2.27 (m, 1H), 0.91 (d, 6H); MS (ES+): m/z 334 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722901B2
出典データセットuspto-grants-2014_05
ORD IDord-daf9ccc5ba91423eab22caed2f04b704
出典メモuspto-grants-2014_05