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HRID 77029作成日:2026年10月24日

Dicyclohexylcarbodiimide → HCID 59401250、化合物

https://huagongshe.com/ja/reaction/77029

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物alpha-(Phenylamino)benzeneacetic acidHCID 19375—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1-Methylazepan-4-olHCID 10975509—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 59401250HCID 5940125020.3%

反応手順

A mixture of 2-phenyl-2-(phenylamino)acetic acid (I1) (175 mg, 0.77 mmol), DCC (192 mg, 0.92 mmol), HOBt (124 mg, 0.92 mmol) and 1-methyl-azepan-4-ol (100 mg, 0.77 mmol) in dry THF (100 mL) is stirred at RT overnight under nitrogen flowstream (UPLC-MS monitoring: complete conversion). The solvent is evaporated and the residue is taken up with aq. HCl and washed with EtOAc. The aqueous phase is basified with NaHCO3 and extracted with DCM (three times). The organic layers are combined, dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is first purified by flash chromatography (DCM to DCM/MeOH=95/5) and then by preparative LC-MS. The purified compound is partitioned between sat. NaHCO3 and DCM, the organic phase is dried over Na2SO4, filtered and evaporated under vacuum to give 53 mg of the title compound as brown oil (20% yield, mixture of diastereoisomers).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835682B2
出典データセットuspto-grants-2014_09
ORD IDord-0605cbee109747b89d917af46f3abb88
出典メモuspto-grants-2014_09