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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46317Generated: October 26, 2026

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

https://huagongshe.com/reaction/46317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4-Thiadiazol-2-amineHCID 19909—
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystHCID 178460663HCID 178460663—
SolventDichloromethaneHCID 6344—
ProductN-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 5804227845%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-015316899b3a4942a482a9e33c8ef297
Source noteuspto-grants-2013_09