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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825802Generated: November 1, 2026

Potassium Carbonate → 4-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-phenothiazine-10-carboxylic Acid tert-Butyl Ester

https://huagongshe.com/reaction/1825802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-morpholinopyran-4-oneHCID 6605262—
Reactant4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenothiazine-10-carboxylic acid tert-butyl esterHCID 23574570—
Solvent1,4-DioxaneHCID 31275—
Product4-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-phenothiazine-10-carboxylic Acid tert-Butyl EsterHCID 23574571100.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

Powdered potassium carbonate (2.03 g, 14.68 mmol) and 2-Chloro-6-morpholin-4-yl-pyran-4-one (1.44 g, 6.70 mmol) were added to a stirred solution of 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenothiazine-10-carboxylic acid tert-butyl ester (2.85 g, 6.70 mmol) in anhydrous dioxane (20 ml) and the mixture degassed (sonication for 20 minutes then saturated with N2) thoroughly. Tetrakis (triphenylphosphine) palladium was then added in a single portion and the mixture degassed (sonication for 20 minutes then saturated with N2) once again before a reflux condenser was attached and the mixture heated to 100° C. under a nitrogen atmosphere for 20 hours. Water (30 ml) was added and the mixture extracted with EtOAc (3×30 ml). The organic extracts were then dried using MgSO4, filtered and concentrated in vacuo to yield a dark brown, crystalline solid (3.21 g, 100%) that was taken forward with no further purification. m/z (LC-MS, ESP): 479 [M+H]+, R/T=4.55 mins

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049313B2
Source datasetuspto-grants-2006_05
ORD IDord-2afa5eb586d949d7bf6808f5d648dd4d
Source noteuspto-grants-2006_05