HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 11328505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23039512 | HCID 23039512 | — |
| Reactant | (6-Iodopyridin-3-yl)methanol | HCID 23039516 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11328505 | HCID 11328505 | — |
| Product | HCID 15022134 | HCID 15022134 | — |
Reaction Steps
In 10 ml of N,N-dimethylformamide were dissolved 1.4 g of 2-(2-chloro-2-methylpropyl)-4,5-dichloro-3(2H)-pyridazinone and 1.29 g of 2-iodo-5-pyridyl methanol, and thereto was added 0.33 g of powdery potassium hydroxide under ice-cooling. The mixture solution was stirred for one day at room temperature. Then, the procedures in Preparation Example 2 were repeated to give 0.74 g of 4-chloro-2-(2-chloro-2-methylpropyl)-5-[(2-iodo-5-pyridyl)methoxy]-3(2H)-pyridazinone (m.p.: 119°-123° C.) and 0.24 g of 4-chloro-5-[(2-iodo-5-pyridyl)-methoxy]-2-(2-methyl-1-propenyl)-3(2H)-pyridazinone (m.p.: 141°-142° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04945091 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-25616024440c4e438f80594b1751506b |
| Source note | uspto-grants-1990_07 |