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HRID 76982作成日:2026年10月24日

Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetate

https://huagongshe.com/ja/reaction/76982

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-Quinuclidinol, (-)-HCID 91404—
反応物Phenyl-o-methylphenylamino-acetic acid hydrochlorideHCID 67124826—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetateHCID 46840573103%

反応手順

PS-DCC (1.15 g, 1.44 mmol, loading: 1.25 mmol/g) is suspended in THF (15 mL). Phenyl-o-methylphenylamino-acetic acid hydrochloride (I38) (200 mg, 0.72 mmol) and HOBT (221 mg, 1.44 mmol) are added, followed by (R)-quinuclidin-3-ol (275 mg, 2.16 mmol) and the mixture is shaken for 16 hours at RT. PS-DCC is filtered off and the filtrate is evaporated. The resulting residue is dissolved in EtOAc and washed sequentially with water, sat. NaHCO3, water and brine. The organic layer is dried over Na2SO4, filtered and evaporated to give the title compound as a colorless oil (260 mg, quantitative 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-fa2f4e8b8cfa400a9064e04cb8dbcc6a
出典メモuspto-grants-2014_09