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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1295236생성일: 2026년 10월 26일

Water → 2-(2-Phenyl-4-thiazolylmethoxy)-5-pyridylmethanol

https://huagongshe.com/reaction/1295236

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Methyl 6-chloropyridine-3-carboxylateHCID 254249—
반응물4-(Hydroxymethyl)-2-phenyl-1,3-thiazoleHCID 2776473—
용매DimethylformamideHCID 6228—
생성물2-(2-Phenyl-4-thiazolylmethoxy)-5-pyridylmethanolHCID 2293074156%

반응 단계

To a solution of 2-phenyl-4-thiazolylmethanol (6.69 g) and methyl 6-chloro-3-pyridinecarboxylate (6.01 g) in N,N-dimethylformamide (100 ml) was added sodium hydride (60% in oil, 1.40 g) at 0° C. and the mixture was stirred for 30 min. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. To a solution of the residue in tetrahydrofuran (150 ml) was added aluminum lithium hydride (1.33 g) at 0° C. and the mixture was stirred at room temperature for 10 min. Sodium sulfate 10 hydrate (11.3 g) was added to the reaction mixture and the mixture was stirred at room temperature for 30 min. The precipitate was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 2-(2-phenyl-4-thiazolylmethoxy)-5-pyridylmethanol (5.81 g, yield 56%) was obtained as colorless crystals from a fraction eluted with tetrahydrofuran. The crystals were recrystallized from tetrahydrofuran-hexane. melting point: 134–135° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241785B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-bd5f74b670074eb7a2c94cc58f7a31bb
출처 메모uspto-grants-2007_07