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HRID 412474作成日:2026年10月24日

Diisopropylethylamine → (R)-3-[4-({(4-tert-butylcyclohexyl)-[2-(4-trifluoromethoxyphenyl)acetyl]amino}methyl)benzoylamino]-2-hydroxypropionic acid

https://huagongshe.com/ja/reaction/412474

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物PyBroPHCID 2733179—
反応物2-[4-(Trifluoromethoxy)phenyl]acetic acidHCID 2777319—
反応物(R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acidHCID 67485259—
溶媒1,2-DichloropropaneHCID 6564—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(R)-3-[4-({(4-tert-butylcyclohexyl)-[2-(4-trifluoromethoxyphenyl)acetyl]amino}methyl)benzoylamino]-2-hydroxypropionic acidHCID 10370959—

反応条件

温度25 °C

反応手順

The above resin bound (R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acid was added 1,2-dichloropropane (500 μL) and BSA (100 μL) and the mixture was vortexed at 25° C. for 1 hour followed by filtration. To the resin was added a solution of 4-(trifluoromethoxy)phenylacetic acid (400 umol) in a mixture of N-methyl-2-pyrrolidinone, 1,2-dichloropropane and diisopropylethylamine (4.5:4.5:1, 1 mL) was added followed by a solution of bromo-tris(pyrrolidino)phosphonium hexafluorophosphate (400 μmol) in 1,2-dichloropropane (500 μL). The mixture was allowed to react for 3 hours at 50° C. and the resin was allowed to cool to 25° C. while washed with N-methyl-2-pyrrolidinone (4×1 mL), and DCM (10×1 mL) afforded the resin bound title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562807B2
出典データセットuspto-grants-2003_05
ORD IDord-befc34fa7ab04dc0bd504b10c5b3a411
出典メモuspto-grants-2003_05