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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2102319생성일: 2026년 10월 26일

Sodium Hydroxide → 3-(beta-d-Glucopyranosyloxy)-4-[(4-methylthiophenyl)methyl]-1h-pyrazole

https://huagongshe.com/reaction/2102319

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물alpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
반응물4-[(4-Methylthiophenyl)methyl]-5-phenyl-1,2-dihydro-3h-pyrazole-3-oneHCID 66971062—
촉매Benzenemethanaminium, N,N,N-tributyl-, bromideHCID 2724282—
용매DichloromethaneHCID 6344—
생성물3-(beta-d-Glucopyranosyloxy)-4-[(4-methylthiophenyl)methyl]-1h-pyrazoleHCID 17850314629.4%

반응 단계

To a suspension of 4-[(4-methylthiophenyl)methyl]-5-phenyl-1,2-dihydro-3H-pyrazole-3-one (0.087 g), acetobromo-α-D-glucose (0.62 g) and benzyltri(n-butyl)ammonium bromide (0.054 g) in dichloromethane (3 mL) was added a sodium hydroxide aqueous solution (5 mol/L, 0.9 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was purified by column chromatography on aminopropylated silica gel (eluent: tetrahydrofuran). The obtained semi purified 4-[(4-methylthiophenyl)methyl]-3-(2,3,4,6-tetraacethyl-β-D-glucopyranosyloxy)-1H-pyrazole was dissolved in methanol (5 mL), and sodium methoxide (28% methanol solution, 0.28 mL) was added to the solution. The mixture was stirred at room temperature for 2 hours. Acetic acid (0.090 g) was added to the reaction mixture, and the solvent was removed. Water (5 mL) was added to the residue, and the mixture was purified by solid phase extraction on ODS (washing solvent: water/methanol=5/1, eluent: methanol). Column chromatography on silica gel (eluent: dichloromethane/methanol=20/1-7/1) was used for further purification to give the title compound (0.033 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07576063B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-123539307f5a47ba9d770d4f37f6024a
출처 메모uspto-grants-2009_08