HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenothiazine → HCID 13238937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 2-Iodopyridine | HCID 221126 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 13238937 | HCID 13238937 | 70% |
Reaction Steps
To start with, 2.35 g (11.8 mmol) of phenothiazine (product of Tokyo Kasei Kogyo Co., Ltd.), 3.63 g (17.7 mmol) of 2-iodopyridine (product of Tokyo Kasei Kogyo Co., Ltd.), 6.5 g of potassium carbonate, 1.5 g of copper powder, and 0.31 g of 18-crown-6-ether were mixed with the use of 20 ml of o-dichlorobenzene as a solvent, followed by reflux under a nitrogen atmosphere for 16 hours. After that, copper and inorganic salt were removed and then column purification using a toluene solvent was performed to give a ligand ppt (10-(2-pyridyl)phenothiazine) (opaque white powder; yield: 70%). A summary of the synthesis scheme is shown in the following (a-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176307B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-4032f55d645943beae291fa9439de2c9 |
| Source note | uspto-grants-2007_02 |