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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417195생성일: 2026년 10월 25일

Hydrochloric Acid → rac-(2'S,3'R,4'S,5'R)-6-chloro-4'-(3-chloro-2-fluoro-phenyl)-2'-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-5'-carboxylic acid (2-oxo-1-propyl-1,2-dihydro-pyridin-4-yl)-amide

https://huagongshe.com/reaction/417195

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물rac-(2'S,3'R,4'S,5'R)-6-chloro-4'-(3-chloro-2-fluoro-phenyl)-2'-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-5'-carboxylic acid {1-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2-dihydro-pyridin-4-yl}-amideHCID 76741121—
생성물rac-(2'S,3'R,4'S,5'R)-6-chloro-4'-(3-chloro-2-fluoro-phenyl)-2'-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3'-pyrrolidine]-5'-carboxylic acid (2-oxo-1-propyl-1,2-dihydro-pyridin-4-yl)-amideHCID 77154983—

반응 단계

To a solution of rac-(2′S,3′R,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carboxylic acid {1-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2-dihydro-pyridin-4-yl}-amide (0.1 g, 0.14 mmol) in tetrahydrofuran (3 mL) was added aqueous HCl solution (1N, 3 mL, 3 mmol). The reaction mixture was stirred at room temperature for 1 h. The mixture was concentrated. The residue was partitioned between ethyl acetate and aqueous saturated NaHCO3 solution. The organic layer was separated, washed with water, brine, dried over Na2SO4, then concentrated. The residue was purified by chromatography (10-15% of MeOH in EtOAc) to give rac-(2′S,3′R,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carboxylic acid (2-oxo-1-propyl-1,2-dihydro-pyridin-4-yl)-amide as a white solid (Yield, 12 mg, 14%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088815B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-350cae2ac52344e498190e6219666499
출처 메모uspto-grants-2012_01