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HRID 46317Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/46317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3,4-Thiadiazol-2-amineHCID 19909—
Edukt2,4-DimethoxybenzaldehydeHCID 69175—
EduktSodium triacetoxyborohydrideHCID 5049666—
KatalysatorHCID 178460663HCID 178460663—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227845%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541588B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-015316899b3a4942a482a9e33c8ef297
Quellennotizuspto-grants-2013_09