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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426384Generated: November 1, 2026

Triazabicyclodecene → [1-(3-Fluoro-4-methyl-benzyl)-piperidin-4-yl]-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine

https://huagongshe.com/reaction/1426384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriazabicyclodeceneHCID 79873—
Reactant3-Fluoro-4-methylbenzyl bromideHCID 2774603—
ReactantPiperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amineHCID 59323569—
SolventAcetonitrileHCID 6342—
Product[1-(3-Fluoro-4-methyl-benzyl)-piperidin-4-yl]-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amineHCID 2505494245.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine (D4) (0.025 g, 0.1 mmol), 3-fluoro-4-methylbenzyl bromide (0.012 ml, 0.11 mmol) and polymer supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (2.9 mmol/g) (0.102 g, 0.30 mmol) in acetonitrile (3 ml) was stirred at 80° C. for 30 min. After cooling to room temperature, the reaction mixture was filtered through an Isolute SCX-2 cartridge. The cartridge was then washed with methanol. The crude product was eluted with a 7M solution of ammonia in methanol. The solvent was evaporated in vacuo. The crude product was purified by flash column chromatography (silica gel; 5% ammonia in methanol (7M)/dichloromethane) to yield E9 (0.017 g, 45%) as a solid. C16H18F4N4S requires 374. Found 375 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933101B2
Source datasetuspto-grants-2015_01
ORD IDord-d2f0d658ea3840c69315bdb6f6849660
Source noteuspto-grants-2015_01