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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979078Generated: October 31, 2026

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

https://huagongshe.com/reaction/979078

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 numberUS04666907
Source datasetuspto-grants-1987_05
ORD IDord-cf9825c812814d1dad7101d844794a0f
Source noteuspto-grants-1987_05