HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → [5-Ethyl-6-(furan-2-yl)-pyrimidin-4-yl]-hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Chloro-5-ethyl-6-(furan-2-yl)-pyrimidine | HCID 65645416 | — |
| Solvent | Water | HCID 962 | — |
| Product | [5-Ethyl-6-(furan-2-yl)-pyrimidin-4-yl]-hydrazine | HCID 67814467 | 97.1% |
Reaction Steps
A mixture of 4-chloro-5-ethyl-6-(furan-2-yl)-pyrimidine (3.0 g), hydrazine monohydrate (3.0 g), triethylamine (3.0 g), and THF (20 ml) was stirred under reflux for 2 hours. To the mixture, hydrazine monohydrate (1 g) was added, and stirred under reflux for 3 hours. After standing to cool the reaction mixture to room temperature, to the reaction mixture, water was added, and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure to give 2.85 g of [5-ethyl-6-(furan-2-yl)-pyrimidin-4-yl]-hydrazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09089136B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-19306e042661451f8b644e57485b585c |
| Source note | uspto-grants-2015_07 |