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HRID 2091625作成日:2026年10月27日

Acetic Acid → (S)-4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(5-(4-(3-methylbutan-2-yl)-4H-1,2,4-triazol-3-yl)thiophen-3-yl)picolinamide

https://huagongshe.com/reaction/2091625

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1,2-Dimethylpropylamine, (S)-HCID 6999788—
反応物4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(5-(hydrazinecarbonyl)thiophen-3-yl)picolinamideHCID 58035645—
溶媒TolueneHCID 1140—
生成物(S)-4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(5-(4-(3-methylbutan-2-yl)-4H-1,2,4-triazol-3-yl)thiophen-3-yl)picolinamideHCID 5659739342%

反応条件

温度150 °C

反応手順

A mixture of 4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(5-(hydrazinecarbonyl)thiophen-3-yl)picolinamide (130 mg, 0.35 mmol) and toluene (2 mL) were added to a sealable vial. N,N-dimethylformamide/N,N-dimethylacetamide complex (120 μL, 0.88 mmol) was added and the reaction was stirred for 5 minutes. (S)-3-methylbutan-2-amine (170 μL, 1.4 mmol), and acetic acid (20 μL, 0.35 mmol) were added, and the reaction was heated in a microwave reactor at 150° C. for 30 minutes. The reaction was concentrated and purified by RP-HPLC to provide 65 mg (42%) of (S)-4-(4-cyclopropyl-1H-imidazol-1-yl)-N-(5-(4-(3-methylbutan-2-yl)-4H-1,2,4-triazol-3-yl)thiophen-3-yl)picolinamide as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08440665B2
出典データセットuspto-grants-2013_05
ORD IDord-002925850de240dd8f25e7aaf84d5f55
出典メモuspto-grants-2013_05