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HRID 46318作成日:2026年10月27日

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

https://huagongshe.com/reaction/46318

反応式

関与物質

役割名称HCID仕込み量
反応物1,3,4-Thiadiazol-2-amineHCID 19909—
反応物2,4-DimethoxybenzaldehydeHCID 69175—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒O-XyleneHCID 7237—
溶媒2-MethyltetrahydrofuranHCID 7301—
生成物N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227873.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541588B2
出典データセットuspto-grants-2013_09
ORD IDord-af710dbdaf82476fa13e16dd34a0e920
出典メモuspto-grants-2013_09