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HRID 391548作成日:2026年10月26日

N-(3-ethynylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide → (S)-5-[(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}phenyl)ethynyl]-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]nicotinamide

https://huagongshe.com/reaction/391548

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-ethynylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 57657904—
反応物(S)-5-bromo-N-[methyl(oxido)phenyl--sulfanylidene]nicotinamideHCID 86629466—
生成物(S)-5-[(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}phenyl)ethynyl]-N-[methyl(oxo)phenyl-lambda6-sulfanylidene]nicotinamideHCID 2495349064%

反応手順

In a manner similar to that described in Example 449, 2,5-Dimethyl-2H-pyrazole-3-carboxylic acid (3-ethynyl-phenyl)-amide (0.0354 g, 0.222 mmol) and (S)-5-bromo-N-[methyl(oxo)phenyl-λ6-sulfanylidene]nicotinamide (0.050 g, 0.148 mmol) were reacted to give the title compound as a white solid (47 mg, 64%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383825B2
出典データセットuspto-grants-2013_02
ORD IDord-126f990af55c48af9a9dd68d34a1846a
出典メモuspto-grants-2013_02