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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49755Generated: October 29, 2026

1-Methylpiperazine → 9-(4-Methyl-piperazin-1-yl)-4-thia-10a-aza-benzo[f]azulene

https://huagongshe.com/reaction/49755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant9,10-Dihydropyrrolo[2,1-b][1,3]benzothiazepin-9-oneHCID 10822568—
SolventWaterHCID 962—
Product9-(4-Methyl-piperazin-1-yl)-4-thia-10a-aza-benzo[f]azuleneHCID 979625584%

Reaction Steps

A solution of 9,10-dihydropyrrolo[2,1-b][1,3]benzothiazepin-9-one (0.24 g, 1.11 mmol), N-methylpiperazine (0.55 mL, 0.50 g, 4.99 mmol) and trimethylsilyl triflate (0.55 mL, 0.68 g, 3.05 mmol) was heated at 120° C. under stirring, after a few minutes further 0.55 mL of N-methylpiperazine were added and the reaction was kept for 3 hours at 120° C. After that time water was added and was extracted with dichloromethane. The organic layer was dried over sodium sulphate, filtered and evaporated to give the crude product that was purified by means of a flash chromatography (20% methanol in ethyl acetate) to afford 0.114 g of the pure title compound as a yellowish solid (84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710041B2
Source datasetuspto-grants-2004_03
ORD IDord-839aa6d361804ea2a67fc94a608c6737
Source noteuspto-grants-2004_03