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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7314생성일: 2026년 10월 24일

Hydrochloric Acid → N-[(6-Chloro-2-naphthyl)sulfonyl]-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}glycine

https://huagongshe.com/ko/reaction/7314

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HydroxideHCID 3939—
반응물Methyl N-[(6-chloro-2-naphthyl)sulfonyl]-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}glycinateHCID 69329776—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Hydrochloride methanolHCID 2189372610%
생성물N-[(6-Chloro-2-naphthyl)sulfonyl]-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}glycineHCID 69329589205.4%

반응 단계

To a solution of methyl N-[(6-chloro-2-naphthyl)sulfonyl]-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}glycinate (0.010 g) in THF (1 ml) was added lithium hydroxide (0.005 g) in water (1 ml), and the resultant solution stirred for 16 h. The mixture was acidified to pH5 using hydrochloric acid (2N), and then concentrated under reduced pressure. The residue was purified using SPE (eluting with methanol and then 10% HCl/methanol) to give the title compound (0.01 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084139B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-49ce8660a0d44e569b4a46c3a121a7e7
출처 메모uspto-grants-2006_08