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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231044Generated: October 27, 2026

Dimethylformamide → 4-chloro-3-methoxy-10-methyl-10H-phenothiazine

https://huagongshe.com/reaction/231044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-chloro-3-hydroxy-10H-phenothiazineHCID 9881418—
SolventMethanolHCID 887—
Product4-chloro-3-methoxy-10-methyl-10H-phenothiazineHCID 13882027—

Reaction Steps

To 25 ml of DMF was added methyl iodide (2.9 ml), 4-chloro-3-hydroxy-10H-phenothiazine (see Example 3) (2.3 g) and sodium hydride (0.672 g). The resulting reaction mixture was stirred at ambient temperature for 12 hours. At 0° C., MeOH was added to destroy the remaining hydride, then H2O. The resulting solution was extracted with ethyl acetate and the organic phase, dried and evaporated. The resulting residue was then purified by chromatography on silica gel to give 1.5 g of 4-chloro-3-methoxy-10-methyl-10H-phenothiazine (m.p.: 136° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845083
Source datasetuspto-grants-1989_07
ORD IDord-3ca45229dee74b15b5ff8be4ddb772df
Source noteuspto-grants-1989_07