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HRID 1698917作成日:2026年10月25日

2-(N-methylcarbamoyl)-5-tert-butyl-3-nitropyrrole → 2-(N-methylcarbamoyl)-3-amino-5-tert-butylpyrrole

https://huagongshe.com/reaction/1698917

反応式

関与物質

役割名称HCID仕込み量
反応物2-(N-methylcarbamoyl)-5-tert-butyl-3-nitropyrroleHCID 18322357—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物2-(N-methylcarbamoyl)-3-amino-5-tert-butylpyrroleHCID 18322385781%

反応手順

To a solution of 2-(N-methylcarbamoyl)-5-tert-butyl-3-nitropyrrole (1.0 g, 0.4 mmol) in EtOAc (50 mL) under an Ar atmosphere was added 10% Pd/C (50 mg). The mixture was evacuated then placed under a static H2 atmosphere (1 atm.) for 24 h. The resulting slurry was filtered through a pad of Celite® with the aid of EtOAc, and the filtrate was concentrated under reduced pressure to afford 2-(N-methylcarbamoyl)-3-amino-5-tert-butylpyrrole (0.61 g, 70%): 1H-NMR (DMSO-d6) δ1.16 (s, 9H), 2.66 (d, J=4.41 Hz, 3H), 4.89 (br s, 2H), 5.27 (d, 2.58 Hz, 1H), 7.14-7.16 (m, 1H), 9.52 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06344476B1
出典データセットuspto-grants-2002_02
ORD IDord-cd8d8d96f0094c83b3f658e5ae260fed
出典メモuspto-grants-2002_02