HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426382Generated: November 1, 2026
4-Fluorobenzyl chloride → [1-(4-Fluoro-benzyl)-piperidin-4-yl]-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine
https://huagongshe.com/reaction/1426382
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine | HCID 59323569 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [1-(4-Fluoro-benzyl)-piperidin-4-yl]-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine | HCID 25054684 | 73% |
Reaction Steps
A mixture of piperidin-4-yl-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-amine (D4) (0.040 g, 0.16 mmol), 4-fluorobenzyl chloride (0.023 ml, 0.19 mmol) and diisopropylethylamine (0.042 ml, 0.24 mmol) in acetonitrile (3 ml) was stirred at 120° C. for 30 min., under microwave irradiation. After cooling to room temperature, the reaction mixture was diluted with dichloromethane and extracted with a 10% solution of ammonium chloride (25 ml). The organic layer was separated, dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (silica gel; 0-3% ammonia in methanol (7M)/dichloromethane) to yield E4 (0.042 g, 73%) as a solid. C15H16F4N4S requires 360. Found 361 (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-afbbb94f430341bc885eaf9bc3c299cd |
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| Source note | uspto-grants-2015_01 |
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