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HRID 46317作成日:2026年10月25日

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

https://huagongshe.com/reaction/46317

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 triacetoxyborohydrideHCID 5049666—
触媒HCID 178460663HCID 178460663—
溶媒DichloromethaneHCID 6344—
生成物N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227845%

反応手順

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.

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-015316899b3a4942a482a9e33c8ef297
出典メモuspto-grants-2013_09