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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808190Generated: November 1, 2026

Triethylamine → N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/1808190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantSodium borohydrideHCID 4311764—
Reactant1,2,4-Thiadiazol-3-amineHCID 20249664—
CatalystPiperidineHCID 8082—
CatalystChlorotitaniumtriisopropoxideHCID 11673339—
SolventDichloromethaneHCID 6344—
SolventHeptaneHCID 8900—
SolventSodium BicarbonateHCID 516892—
ProductN-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amineHCID 5773221618.3%

Reaction Steps

2,4 Dimethoxybenzaldehyde (4.1 g, 24 mmol, 1 eq), 2 amino-1,2,4-thiadiazole (2.5 g, 24.7 mmol, 1 eq), Et3N (3.04 g, 30 mmol, 1 eq) and piperidine (25 mg, 0.297 mmol, 0.012 eq) were combined in DCM (100 ml) and the reaction mixture heated to reflux over sieves for 72 hours. The reaction mixture was cooled to room temperature and chlorotitaniumisopropoxide (1M solution in hexane, 29.7 ml, 29.7 mmol, 1.2 eq) was added and the reaction mixture stirred at room temperature for 15 minutes. The sieves were removed by filtration and the reaction mixture diluted with MeOH (50 ml). Sodium borohydride (3.7 g, 99 mmol, 4.0 eq) was added portionwise and the reaction mixture stirred for 1 hour. The reaction mixture was diluted with saturated sodium hydrogen carbonate (100 ml) and the resulting titanium precipitate removed by filtration through Celite. The filtrate was dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was purified by column chromatography eluting with 15-60% ethyl acetate: heptane to yield the title compound (111 g, 4.38 mmol, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-4140acea94b847e2beb0af022f4ef652
Source noteuspto-grants-2013_01