HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675005Generated: October 30, 2026
Diisopropylethylamine → HCID 59149841, compound
https://huagongshe.com/reaction/1675005
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 | HCID 28798584 | HCID 28798584 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59149841 | HCID 59149841 | 85% |
Reaction Steps
6-Chloro-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine (251 mg, 1.13 mmol), (R)-1-[1-(4-bromophenyl)ethyl]piperazine (obtained as described in Example 270, preparation of starting materials, 304 mg, 1.13 mmol) and DIPEA (0.20 mL, 1.13 mmol) in DMF (3 mL) were stirred and heated at 80° C. for 1 hour. The resulting solution was cooled to ambient temperature then quenched with water (10 mL) to give a pale brown precipitate. The precipitate was collected by filtration, washed sequentially with water, acetonitrile and ether and dried under vacuum to afford 6-[4-[(1R)-1-(4-bromophenyl)ethyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine (437 mg, 85%) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003649B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a6688a097ad44f66b109c6098390cbad |
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| Source note | uspto-grants-2011_08 |
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