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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348384Generated: October 29, 2026

Phenothiazine → HCID 13238937, compound

https://huagongshe.com/reaction/348384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenothiazineHCID 7108—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-IodopyridineHCID 221126—
CatalystCopperHCID 23978—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 13238937HCID 1323893770%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176307B2
Source datasetuspto-grants-2007_02
ORD IDord-4032f55d645943beae291fa9439de2c9
Source noteuspto-grants-2007_02