HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Chloro-3-cyclopentyloxy-2-nitro-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Iodocyclopentane | HCID 73784 | — |
| Reactant | 5-Chloro-2-nitropyridin-3-ol | HCID 18765698 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-3-cyclopentyloxy-2-nitro-pyridine | HCID 67486838 | 60% |
Reaction Steps
5-Chloro-2-nitro-pyridine-3-ol (3.4 mmol) is dissolved in DMF (2 ml) and NaH (1.4 eq., 60% suspension in liquid paraffin) is added and the suspension is stirred 45 min at room temperature. Cyclopentyliodide (1 eq.) is added and the reaction suspension is heated to 100° C. for 24 hours. The reaction solution is pored into water and extracted with dichloromethane. The combined organic layers are washed with brine, dried over MgSO4 and the solvent is removed in vacuo. 5-Chloro-3-cyclopentyloxy-2-nitro-pyridine is obtained after column chromatography as yellow oil in a yield of 60%; HPLC (method C): 2.11 min; LC-MS (method A): 2.07 min, 243.10 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420642B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-b16d58a3a939457bb36a68a4731cdf8c |
| Source note | uspto-grants-2013_04 |