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HRID 907358作成日:2026年10月27日

1-Methyl-N-[2-(4-morpholinyl)ethyl]-4-nitro-1H-pyrrole-2-carboxamide → 1-Methyl-4-{[(1-methyl-4-nitro-1H-pyrrol-2-yl)carbonyl]amino}-N-[2-(4-morpholinyl)ethyl]-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/907358

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methyl-N-[2-(4-morpholinyl)ethyl]-4-nitro-1H-pyrrole-2-carboxamideHCID 10989673—
反応物1-Methyl-4-nitro-1H-pyrrole-2-carbonyl chlorideHCID 11063185—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物1-Methyl-4-{[(1-methyl-4-nitro-1H-pyrrol-2-yl)carbonyl]amino}-N-[2-(4-morpholinyl)ethyl]-1H-pyrrole-2-carboxamideHCID 10862348—

反応条件

温度0 °C

反応手順

1-Methyl-N-[2-(4-morpholinyl)ethyl]-4-nitro-1H-pyrrole-2-carboxamide (1.42 g, 3.41 mmol; see step (iii) above) was dissolved in methanol (10 mL) and cooled to 0° C., Pd/C (0.055 g) was then added in small portions and the solution stirred under H2 for 3 h. The solution was then filtered and the solvent removed under reduced pressure. A solution of 1-methyl-4-nitro-1H-pyrrole-2-carbonyl chloride (0.642 g, 3.42 mmol) in DCM (10 mL) was added and the mixture allowed to stir for 1 h at RT. The solvent was then removed under reduced pressure and the crude product was separated on basified silica using a 1:1 solution of methanol ethyl acetate to yield the sub-title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08012967B2
出典データセットuspto-grants-2011_09
ORD IDord-60e0de94851d488a89d4953e9735e5ba
出典メモuspto-grants-2011_09