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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1255011생성일: 2026년 10월 27일

Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetate

https://huagongshe.com/reaction/1255011

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Quinuclidinol, (-)-HCID 91404—
반응물(Benzylamino)Phenylacetic AcidHCID 2826470—
용매TetrahydrofuranHCID 8028—
생성물(R)-quinuclidin-3-yl 2-(benzylamino)-2-phenylacetateHCID 4684041852%

반응 단계

A mixture of 2-(benzylamino)-2-phenylacetic acid (I23) (0.94 g, 3.90 mmol), DCC (0.97 g, 4.70 mmol), HOBt (0.63 g, 4.07 mmol) and 3(R)-quinuclidinol (1.51 g, 11.7 mmol) in dry THF (30 mL) is stirred at room temperature overnight under nitrogen flowstream (LC-MS monitoring: complete conversion). The solvent is evaporated and the residue is taken up with EtOAc and washed twice with water. The organic phase is dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is purified by flash chromatography (DCM/MeOH=98/2, 0.2% NH3(aq.) to 95/5, 0.5% NH3(aq.)) to give a mixture of diastereoisomers 1 and 2 of C24 (231 mg, 52% yield, mixture of diasteroisomers).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08455646B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-170c2435062f4b65a2c5fa2a8d499746
출처 메모uspto-grants-2013_06