HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674980Generated: October 26, 2026
Diisopropylethylamine → HCID 67340727, compound
https://huagongshe.com/reaction/1674980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-3-(trifluoromethyl)-(1,2,4)triazolo(4,3-b)pyridazine | HCID 613657 | — |
| Reactant | tert-butyl (2R,5S)-2,5-dimethylpiperazine-1-carboxylate | HCID 24903576 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67340727 | HCID 67340727 | 76% |
Reaction Steps
A stirred solution of 6-chloro-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine (4.45 g, 20 mmol), (2R,5S)-tert-butyl 2,5-dimethylpiperazine-1-carboxylate (5.14, 24 mmol) and DIPEA (5.14 mL, 30.00 mmol) in DMF (40.0 mL) was heated at 125° C. for 2.5 hours. The reaction mixture was evaporated to dryness, redissolved in DCM and washed sequentially with 1M aqueous K2CO3, water and saturated brine. The organic layer was dried over MgSO4, filtered and evaporated. The crude product was purified by MPLC silica chromatography, eluting with EtOAc. Product fractions were evaporated and triturated with ether. The solid was collected by filtration, washed with ether and dried under vacuum to afford (2R,5S)-tert-butyl 2,5-dimethyl-4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazine-1-carboxylate (6.09 g, 76%) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003649B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-0dcef6418d434871b599b20246ccbc0f |
|---|
| Source note | uspto-grants-2011_08 |
|---|