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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1827005생성일: 2026년 10월 24일

1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose → 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid (3aR, 5aS, 8aS, 8bR)-2,2,7,7-tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-ylmethyl ester

https://huagongshe.com/ko/reaction/1827005

반응식

참여 물질

역할이름HCID투입량
반응물1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranoseHCID 2723629—
반응물3-[1-(3,5-Dimethyl-1h-pyrrol-2-yl)-meth-(z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carbonyl chlorideHCID 87904695—
용매PyridineHCID 1049—
용매TetrahydrofuranHCID 8028—
생성물3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid (3aR, 5aS, 8aS, 8bR)-2,2,7,7-tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-ylmethyl esterHCID 13172459965%

반응 단계

To a solution of 1,2,3,4-di-O-isopropylidene-D-galactopyranose (650 mg, 2.5 mmol) in 1.0 mL of pyridine and 2.0 mL of THF was added a suspension of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carbonyl chloride (150 mg, 0.5 mmol) at 0° C. The reaction mixture was then gradually warmed to room temperature, stirred for 4 h, and concentrated. The residue was triturated with water and washed with ether to give 170 mg (65%) of 3-[1-(3,5-dimethyl-1H-pyrrol-2-yl)-meth-(Z)-ylidene]-2-oxo-2,3-dihydro-indole-1-carboxylic acid (3aR,5aS,8aS,8bR)-2,2,7,7-tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4′,5′-d]pyran-5-ylmethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07053114B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-c267807db604480a9f586d346fb4366b
출처 메모uspto-grants-2006_05