HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-(7-Chloro-4-quinolinyl)-N-(2,3-dimethylcyclohexyl)-1-piperazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 2,3-Dimethylcyclohexylamine | HCID 123507 | — |
| Reactant | 7-Chloro-4-(piperazin-1-yl)quinoline | HCID 738389 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 4-(7-Chloro-4-quinolinyl)-N-(2,3-dimethylcyclohexyl)-1-piperazinecarboxamide | HCID 21101711 | — |
Reaction Steps
As described for example 78, 2,3-dimethyl-cyclohexanamine (154 mg, 1.21 mmol), 4-nitrophenyl chloroformate (244 mg, 1.21 mmol), diisopropyl(ethyl)amine (209 mg, 1.62 mmol), and 7-chloro-4-(piperazin-1-yl)quinoline (200 mg, 0.81 mmol) are reacted affording the title product after flash chromatography with CH2Cl2-MeOH. 1H NMR (DSMO-d6) δ 0.7–0.9 (m, 7H), 1.13–1.92 (m, 8H), 3.2 (m, 1H), 3.6 (br. s, 4H), 3.9 (br. s, 4H), 7.2 (m, 1H), 7.7 (m, 1H), 8.0 (s, 1H), 8.2 (m, 1H), 8.6 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-56d69cdaf8284c3a8e68099ae5b45b0d |
| Source note | uspto-grants-2007_05 |