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HRID 276859作成日:2026年10月25日

Isobutyl chloroformate → But-2-ynoic acid, [4-(3-bromo-phenylamino)-3-cyano-[1,7]naphthyridin-6-yl]-amide

https://huagongshe.com/reaction/276859

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyl chloroformateHCID 62365—
反応物2-Butynoic acidHCID 68535—
反応物6-Amino-4-(3-bromo-phenylamino)-[1,7]naphthyridine-3-carbonitrileHCID 9798006—
反応物But-2-ynoyl chlorideHCID 12714994—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
生成物But-2-ynoic acid, [4-(3-bromo-phenylamino)-3-cyano-[1,7]naphthyridin-6-yl]-amideHCID 572674848.4%

反応手順

To 100 mg of butynoic acid in 5 mL of anhydrous tetrahydrofuran under an inert atmosphere at 0° C. was added 0.23 mL on N-methyl morpholine and 0.15 mL of isobutyl chloroformate. This solution was then added to 150 mg of 6-amino-4-(3-bromo-phenylamino)-[1.7]naphthyridine-3-carbonitrile in 3 mL of pyridine at 0° C. After standing at 0° C. for three days, a second portion of butynoyl chloride was added. After an additional 8 hours the reaction was stripped of solvents on a rotary evaporator and the crude product was purified by flash chromatograph using a gradient of 0-20% methanol/chloroform to give 15 mg of but-2-ynoic acid, [4-(3-bromo-phenylamino)-3-cyano-[1.7]naphthyridin-6-yl]-amide: melting point 255° C. (decomposed); mass spectrum (m/e): M+H 406.1, 408.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355636B1
出典データセットuspto-grants-2002_03
ORD IDord-c42d2ee735ca4af78f7be2183409aa3c
出典メモuspto-grants-2002_03