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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76975생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/76975

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 번호US08835682B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6079384f7ac84a2e9994e0f88a6b5207
출처 메모uspto-grants-2014_09