戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 469450作成日:2026年10月27日

Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-(2-carbamoylthiophen-3-ylamino)-2-phenylacetate

https://huagongshe.com/reaction/469450

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2-(2-Carbamoylthiophen-3-ylamino)-2-phenylacetic acidHCID 58556989—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-quinuclidin-3-yl 2-(2-carbamoylthiophen-3-ylamino)-2-phenylacetateHCID 547639736%

反応手順

A mixture of 2-(2-carbamoylthiophen-3-ylamino)-2-phenylacetic acid (I7) (389 mg, 1.41 mmol), (R)-quinuclidin-3-ol (215 mg, 1.69 mmol), DCC (349 mg, 1.69 mmol) and HOBT (259 mg, 1.69 mmol) in dry THF (5 ml) was stirred at room temperature overnight. THF was evaporated, and the crude product was taken up with EtOAc and washed twice with 2M K2CO3. The organic phase was dried over Na2SO4, filtered and evaporated to dryness. The crude product was purified by preparative HPLC. The fractions with the product are combined and evaporated to dryness. The residue was dissolved in 2M K2CO3 and extracted twice with EtOAc to obtain (R)-quinuclidin-3-yl 2-(2-carbamoylthiophen-3-ylamino)-2-phenylacetate (32 mg, 6% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629160B2
出典データセットuspto-grants-2014_01
ORD IDord-ce04655f38de48979470b15eda76ccc0
出典メモuspto-grants-2014_01