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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658742Generated: October 31, 2026

1-Methylpiperazine → HCID 3041883, compound

https://huagongshe.com/reaction/1658742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 12232369HCID 12232369—
ProductHCID 3041883HCID 3041883—

Reaction Steps

12 g of 2,10-dichloro-7-fluoro-10,11-dihydro-dibenzo[b,f]thiepin are heated for 10 minutes together with 16 g of N-methylpiperazine at an external temperature of 120°-130°. After cooling the reaction mixture is poured on water and extracted with ether. The organic phase is washed with water and subsequently treated with 2 N hydrochloric acid. A precipitate is obtained. The mixture is extracted with ether, made alkaline and subsequently again extracted with ether. The organic phase is washed with water, dried over magnesium sulphate and evaporated. The so-obtained raw 1-(2-chloro-7-fluoro-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-4-methylpiperazine is converted to the corresponding maleate by treatment with maleic acid. The maleat melts at 200° with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966737
Source datasetuspto-grants-1976_06
ORD IDord-6464a597edb64584a82d22adb9e1724a
Source noteuspto-grants-1976_06