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HRID 393440作成日:2026年10月24日

N-methyl-2-pyrrolidone → n-[(2,2-Dichloro-1-methylcyclopropyl)carbonyl]-4-[[(2,4,6-trimethylphenyl)carbonyl]amino]-l-phenylalanine

https://huagongshe.com/ja/reaction/393440

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物DiisopropylethylamineHCID 81531—
反応物2,2-Dichloro-1-methylcyclopropanecarboxylic acidHCID 102621—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物4-[[(2,4,6-trimethylphenyl)sulfonyl]amino]-L-phenylalanineHCID 54451329—
生成物n-[(2,2-Dichloro-1-methylcyclopropyl)carbonyl]-4-[[(2,4,6-trimethylphenyl)carbonyl]amino]-l-phenylalanineHCID 54131599—

反応手順

4-[[(2,4,6-Trimethylphenyl)sulfonyl]amino]-L-phenylalanine on Wang resin (0.30 g, 0.23 mmol), 2,2-dichloro-1-methylcyclopropane carboxylic acid (0.19 g, 1.14 mmol), BOP ((0.50 g, 1.14 mmol) and DIPEA (0.26 mL, 1.5 mmol) in N-methylpyrrolidinone (3 mL) was agitated for 3 hr. The mixture was filtered and the resin was washed with dichloromethane and methanol and was air dried. Treatment with 90% TFA in dichloromethane for 3 min effected cleavage from the resin. The mixture was filtered, the filtrate was concentrated and lyophilized from water to give N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-4-[[(2,4,6-trimethylphenyl)carbonyl]amino]-L-phenylalanine as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06806365B2
出典データセットuspto-grants-2004_10
ORD IDord-ad849bd6f0684d38bb4a769cc773c319
出典メモuspto-grants-2004_10