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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910465Generated: October 26, 2026

Water → 5-(2-((2-(5-Amino-1,3,4-thiadiazol-2-yl)ethyl)amino)ethyl)-1,3,4-thiadiazol-2-amine

https://huagongshe.com/reaction/1910465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,3'-IminodipropionitrileHCID 8149—
ReactantSodium HydroxideHCID 14798—
ReactantThiosemicarbazideHCID 2723789—
SolventTrifluoroacetic acidHCID 6422—
Product5-(2-((2-(5-Amino-1,3,4-thiadiazol-2-yl)ethyl)amino)ethyl)-1,3,4-thiadiazol-2-amineHCID 395075944.5%

Reaction Steps

A mixture of 3,3′-iminodipropionitrile (1.50 g, 12.18 mmol) and thiosemicarbazide (2.22 g, 24.36 mmol) in TFA (10 mL) was heated at 85 for 4.5 h. The reaction was cooled to room temperature and poured into a mixture of ice and water. Sodium hydroxide pellets were added to the mixture until it was basic (pH 14). The white precipitate was collected by suction filtration, rinsed with water and dried to provide 5-(2-((2-(5-amino-1,3,4-thiadiazol-2-yl)ethyl)amino)ethyl)-1,3,4-thiadiazol-2-amine (1005, 1.47 g). 1H NMR (300 MHz, DMSO-d6) δ 6.95 (s, 4H), 2.90 (d, J=6.0 Hz, 4H), 2.83 (d, J=6.3 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604016B2
Source datasetuspto-grants-2013_12
ORD IDord-9b745f66cb134a159944825ce0ccfebd
Source noteuspto-grants-2013_12