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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732768Generated: November 1, 2026

1-Methylpiperazine → HCID 3045791, compound

https://huagongshe.com/reaction/1732768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant7-Trifluoromethyl-8,10-dichloro-10,11-dihydrodibenzo(b,f)thiepineHCID 12374624—
SolventChloroformHCID 6212—
ProductHCID 3045791HCID 304579156%

Reaction Steps

A mixture of 7-trifluoromethyl-8,10-dichloro-10,11-dihydrodibenzo(b,f)thiepine (2.89 g), 1-methylpiperazine (1.8 ml) and chloroform (2.5 ml) was refluxed for 7 hours. The chloroform was evaporated under diminished pressure, the residue dissolved in benzene (30 ml), washed with water, and the benzene layer separated and shaken with an excess of 3 N-HCl. The precipitated hydrochloride was filtered, added to the aqueous layer of the filtrate and the base liberated by addition of ammonium hydroxide. It was extracted with benzene and the conventional work-up procedure yielded 1.93 g (56%) of the crude 7-trifluoromethyl-8-chloro-10-(4-methylpiperazino)-10,11-dihydrodibenzo(b,f)thiepine. Neutralization with maleic acid in ethanol followed by addition of ether yielded the crystalline maleate which was crystallized from ethanol; m.p. 197°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238611
Source datasetuspto-grants-1980_12
ORD IDord-935a7a3f8ffd43babf405a333effcddc
Source noteuspto-grants-1980_12