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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76980생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → (2-methoxy-phenylamino)-phenyl-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester

https://huagongshe.com/ko/reaction/76980

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Quinuclidinol, (-)-HCID 91404—
반응물(2-Methoxy-phenylamino)-phenyl-acetic acid hydrochlorideHCID 67425641—
용매TetrahydrofuranHCID 8028—
생성물(2-methoxy-phenylamino)-phenyl-acetic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)esterHCID 46840572116.8%

반응 단계

PS-DCC (2.05 g, 2.57 mmol, loading: 1.25 mmol/g) is suspended in THF (15 mL) and shaken for few minutes. Then (2-methoxy-phenylamino)-phenyl-acetic acid hydrochloride (I36) (377 mg, 1.28 mmol) and HOBT (393 mg, 2.57 mmol) are added. After 10 minutes, (R)-quinuclidin-3-ol (490 mg, 3.85 mmol) is added and the mixture is shaken at RT for 16 hours (Conversion complete by UPLC/MS-UV). PS-DCC is filtered off and the filtrate is evaporated to dryness. The residue is dissolved in EtOAc and washed with sat. NaHCO3, water and brine. The organic layer is recovered, dried over Na2SO4, filtered and evaporated to afford the title compound as a yellow oil (548 mg, quantitative yield, mixture of diastereoisomers).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835682B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ec03adcaffbf433582cbda769c62efe2
출처 메모uspto-grants-2014_09