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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triazabicyclodecene | HCID 79873 | — |
| Reactant | 3-Fluoro-4-methylbenzyl bromide | HCID 2774603 | — |
| Reactant | Piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine | HCID 59323569 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [1-(3-Fluoro-4-methyl-benzyl)-piperidin-4-yl]-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine | HCID 25054942 | 45.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933101B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-d2f0d658ea3840c69315bdb6f6849660 |
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| Source note | uspto-grants-2015_01 |
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