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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46317생성일: 2026년 10월 25일

1,3,4-Thiadiazol-2-amine → N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/46317

반응식

참여 물질

역할이름HCID투입량
반응물1,3,4-Thiadiazol-2-amineHCID 19909—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물Sodium triacetoxyborohydrideHCID 5049666—
촉매HCID 178460663HCID 178460663—
용매DichloromethaneHCID 6344—
생성물N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227845%

반응 단계

To a solution of 2-amino-1,3,4-thiadiazole (3.05 g, 0.0302 mol) and 2,4-dimethoxy-benzaldehyde (4.55 g, 0.0274 mol) in dichloromethane (125 mL) was added chlorotriisopropoxytitanium (16 mL, 0.067 mol) portionwise over 5 minutes. After stirring for 1 hour, sodium triacetoxyborohydride (11.72 g, 0.05530 mol) was added portion wise and stirred for 24 hours. The reaction was quenched with saturated aqueous sodium bicarbonate solution and adjusted to pH 9 with sodium hydroxide (6 N aqueous solution) and extracted with dichloromethane. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography eluting with methanol:dichloromethane (gradient 0:1 to 1:9, by volume) to afford the title compound as a white solid, 590 mg, 45% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-015316899b3a4942a482a9e33c8ef297
출처 메모uspto-grants-2013_09