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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 733088생성일: 2026년 10월 26일

Sulfuric Acid → 2,2-Dimethyl-3-[4-({[(2'-oxospiro[cyclopentane-1,3'-indol]-1'(2'H)-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoic acid

https://huagongshe.com/reaction/733088

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참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물DichloromethaneHCID 6344—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 2,2-dimethyl-3-[4-({[(2'-oxospiro[cyclopentane-1,3'-indol]-1'(2'H)-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoateHCID 67232986—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물2,2-Dimethyl-3-[4-({[(2'-oxospiro[cyclopentane-1,3'-indol]-1'(2'H)-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoic acidHCID 1199797480%

반응 단계

To a stirred solution of methyl 2,2-dimethyl-3-[4-({[(2′-oxospiro[cyclopentane-1,3′-indol]-1′(2′H)-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoate (170 mg, 0.38 mmol, step 3 of Example 2) in acetic acid (2 mL), H2SO4 (113 mg) in water (2 mL) was added, and the mixture was refluxed for 36 h. The mixture was cooled to room temperature and solid NaHCO3 (500 mg) was added slowly. The resulting mixture was concentrated to give white solid. To the solid, CH2Cl2 (40 mL) was added and stirred for 10 min, dried over MgSO4. The solution was filtered and concentrated and then resulted yellow oil. The oil was chromatographed on a column of silica gel eluting with CH2Cl2/methanol (14:1) to give 130 mg (80%) of the title compound as white solid. Recrystallization from ethyl acetate/diethyl ether gave white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589109B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-6589e84a55e74305a6452d210621256f
출처 메모uspto-grants-2009_09