HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(2-[4-(4-Chloro-phenyl)-piperazin-1-yl]-2-oxo-ethyl)-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Chloroacetyl)-4-(4-chlorophenyl)piperazine | HCID 4053957 | — |
| Reactant | HCID 178468642 | HCID 178468642 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 2-(2-[4-(4-Chloro-phenyl)-piperazin-1-yl]-2-oxo-ethyl)-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester | HCID 58778044 | — |
Reaction Steps
Protocol T was followed using 5-Thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester, K2CO3, 2-Chloro-1-[4-(4-Chloro-phenyl)-piperazin-1-yl]-ethanone and DMF. Column chromatography using a solvent mixture (hexane/ethyl acetate=1.5/1) afforded the title compound. 1H NMR (400 MHz, CDCl3): 7.34–7.38 (m, 1H), 7.24–7.26 (m, 1H), 7.12 (s, 1H), 7.04–7.08 (dd, 1H), 6.96–7.2 (m, 2H), 6.88–6.94 (m, 2H), 4.32–4.42 (q, 2H), 3.52–3.58 (m, 4H), 3.05–3.35 (m, 4H), 1.32–1.42 (m, 3H). 13C NMR (400 MHz, CDCl3): 164.2, 128, 126.8, 126.6, 120.2, 118.4, 115.2, 62.5, 54.2, 50.5, 42.6,44, 14.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157464B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-0ed906cdb03449f3bba84c4de5034f70 |
| Source note | uspto-grants-2007_01 |