HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485853Generated: October 31, 2026
Diisopropylethylamine → HCID 59242666, compound
https://huagongshe.com/reaction/1485853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 6-Chloro-4-phenyl-3-(trifluoromethyl)pyridazine | HCID 59242649 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59242666 | HCID 59242666 | 93% |
Reaction Steps
To a stirred solution of 6-chloro-4-phenyl-3-trifluoromethyl-pyridazine (D3) (7.1 g, 0.0274 mol) and N-Boc-piperazine (5.62 g, 0.0302 mol) in acetonitrile (150 ml) was added diisopropylethylamine (5.1 ml, 0.0302 mol) and the mixture heated at 150° C. for 20 min., under microwave irradiation. After this period, the reaction mixture was diluted with dichloromethane and extracted with water. The organic layer was separated, dried (MgSO4) and the solvents evaporated in vacuo. The crude product was purified by column chromatography (silica; 20% ethyl acetate in heptane, followed by 10% ethyl acetate in dichloromethane). After evaporation of the solvent, the crude product was crystallised from heptane to yield D4 (10.4 g, 93%). C20H23F3N4O2 requires 408; Found 409 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422296B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-77c3d811a315493ea83f992e39739e7b |
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| Source note | uspto-grants-2016_08 |
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