HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 21071040, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Chloroacetyl)-4-(4-fluorophenyl)piperazine | HCID 1848511 | — |
| Reactant | 3,5-Diisopropylpyrazole | HCID 5255229 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 21071040 | HCID 21071040 | — |
Reaction Steps
Protocol T was followed using 3,5-Diisopropyl-1H-pyrazole, K2CO3, 2-Chloro-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1/1) afforded the title compound as white solid. 1H NMR (400 MHz, CDCl3): 6.92–7.0 (m, 2H), 6.80–6.88 (dd, 2H), 5.88 (s, 1H), 4.92 (s, 2H), 3.70–3.80 (t, 4H), 2.90–3.10 (m, 4H), 1.40–1.60 (m, 12H). 13C NMR (400 MHz, CDCl3): 160.6, 158.2, 150.2, 119.2, 118.0, 100.0, 50.8, 50.5, 50.2, 45.2, 42, 28.2, 26.0, 22.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157464B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-23c2ff44c3174f94a1a199e8bfcdecf9 |
| Source note | uspto-grants-2007_01 |