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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46318생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/46318

반응식

참여 물질

역할이름HCID투입량
반응물1,3,4-Thiadiazol-2-amineHCID 19909—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
용매WaterHCID 962—
용매O-XyleneHCID 7237—
용매2-MethyltetrahydrofuranHCID 7301—
생성물N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227873.5%

반응 단계

2,4-Dimethoxybenzaldehyde (771.37 g, 4.64 moles) was added to a suspension of 2-amino-1,3,4-thiadiazole (391.2 g, 3.87 moles) in xylene (5.87 L) and heated to reflux. Dean-Stark apparatus was used to remove the water and the reaction was stirred overnight. After cooling to room temperature, the reaction was further cooled to 5° C. and diluted with 2-methyltetrahydrofuran (2.93 L). Sodium tetrahydroborate (73.17 g, 1.93 moles) was added as a single portion. Methanol (782.8 mL) was then added slowly over 30 minutes, maintaining the temperature below 15° C. After a further 30 minutes water (1 L) was added followed by saturated aqueous sodium hydrogencarbonate solution (1 L) and the mixture stirred at room temperature overnight. The biphasic mixture was diluted with 2-methyltetrahydrofuran and heated to 43° C. to aid dissolution. The layers were separated and the organic layer washed with water (3 L) before concentrating in vacuo. The resulting solid was slurried in heptanes (2.5 L), homogenised, filtered, washed with tert-butylmethyl ether and dried to afford 715 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-af710dbdaf82476fa13e16dd34a0e920
출처 메모uspto-grants-2013_09