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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2383923생성일: 2026년 10월 27일

Methanol → 3-(3-Benzothiazol-6-yl-2-oxo-imidazolidin-1-yl)-pyridine-4-carbaldehyde

https://huagongshe.com/reaction/2383923

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물p-Toluenesulfonic acidHCID 6101—
반응물1-Benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 49872452—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물3-(3-Benzothiazol-6-yl-2-oxo-imidazolidin-1-yl)-pyridine-4-carbaldehydeHCID 5963627299.5%

반응 단계

PTSA (2.2 g, 11.672 mmol) was added to a stirred solution of 1-benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-one (I-177a: 460 mg, 1.2418 mmol) in acetone (20 mL) and water (20 mL). The resulting reaction mass was stirred for 48 hours at room temperature. The reaction was monitored by TLC (5% methanol in chloroform). The reaction mixture was concentrated, the residue was diluted with ice-water, basified with saturated NaHCO3 solution and extracted using ethyl acetate. The aqueous layer was filtered and the solid collected was dried under reduced pressure. The solid was dissolved in methanol and chloroform, dried over Na2SO4 and concentrated under reduced pressure to afford 400 mg of the product (99.5% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08263635B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-73b9021cf1714944acb1183ab0fcd82f
출처 메모uspto-grants-2012_09