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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76973생성일: 2026년 10월 24일

Hydrochloric Acid → (S)-3-phenyl-2-phenylamino-propionic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl) ester

https://huagongshe.com/ko/reaction/76973

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Quinuclidinol, (-)-HCID 91404—
반응물3-Phenyl-2-(phenylamino)propanoic acidHCID 13416411—
용매TetrahydrofuranHCID 8028—
용매1,4-DioxaneHCID 31275—
생성물(S)-3-phenyl-2-phenylamino-propionic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl) esterHCID 4684041720%

반응 단계

To a solution of 3-phenyl-2-(phenylamino)propanoic acid (I21) (1.21 g, 5.01 mmol) in dioxane, a 4M solution of HCl in dioxane (5 mL) is added and the reaction is allowed to stir at RT for 1 hour; the solvent is evaporated under reduced pressure to obtain a white solid which is dissolved in dry THF (70 mL). DCC (1.22 g, 6.01 mmol), HOBt (0.8 g, 6.0 mmol) and 3(R)-quinuclidinol (1.31 g, 10.1 mmol) are added to the resulting solution and the mixture stirred for 24 hours at RT under nitrogen flowstream (LC-MS monitoring: complete conversion). The solvent is evaporated. 1N HCl (20 mL) is added to the resulting crude and the aqueous layer is washed with EtOAc (2×50 mL); NaHCO3 is added to the aqueous layer (pH=7-8) and the product is extracted with DCM and dried over Na2SO4, to obtain 530 mg (35% yield) of diastereoisomer 1 of C22, which is further purified by preparative LC-MS to get the titled product as a brown oil (mixture of diastereoisomers that contains 20% of diastereoisomer 2 of C22, TFA salt).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835682B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e84dc1e953274299b9d00d88c4ff9782
출처 메모uspto-grants-2014_09