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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1994758생성일: 2026년 10월 26일

Dimethylformamide → N-methyl-N-(2-{5-[(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-8-yl)methyl]-1,3-thiazol-2-yl}-1H-indol-7-yl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1994758

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물1-Oxa-3,8-diazaspiro(4.5)decan 2-oneHCID 12954114—
반응물N-{2-[5-(chloromethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylthiophene-2-sulfonamideHCID 57475969—
용매WaterHCID 962—
생성물N-methyl-N-(2-{5-[(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-8-yl)methyl]-1,3-thiazol-2-yl}-1H-indol-7-yl)thiophene-2-sulfonamideHCID 5913612543%

반응 단계

A mixture of N-{2-[5-(chloromethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylthiophene-2-sulfonamide (150 mg), triethylamine (150 μL), 1-oxa-3,8-diazaspiro[4.5]decan-2-one (110 mg) and N,N-dimethylformamide (2 ml) was stirred at room temperature for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (82 mg, yield 43%) as colorless crystals from a fraction eluted with ethyl acetate. melting point 224° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652133B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-124b652828014b7dac8bb8e567e24c98
출처 메모uspto-grants-2010_01