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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087555Generated: November 1, 2026

Sodium Chloride → 1-methyl-4-[(7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizin-10-yl)carbonyl]piperazine

https://huagongshe.com/reaction/1087555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantThionyl ChlorideHCID 24386—
Reactant1-MethylpiperazineHCID 53167—
Reactant7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxylic acidHCID 14666743—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-methyl-4-[(7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizin-10-yl)carbonyl]piperazineHCID 14770076—

Reaction Steps

1.93 g of 7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizine-10-carboxylic acid were converted into the acid chloride with 2.65 ml of thionyl chloride as described. This acid chloride was taken up in 80 ml of dioxane, treated with 2.7 ml of N-methylpiperazine, and the mixture was then stirred at room temperature until the reaction was completed and poured into 200 ml of water. The aqueous phase was saturated with sodium chloride and extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and evaporated. By recrystallization from toluene there was obtained 1-methyl-4-[(7-oxo-8-phenyl-7H-thieno[2,3-a]quinolizin-10-yl)carbonyl]piperazine as yellow crystals of m.p. 233°-234° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036066
Source datasetuspto-grants-1991_07
ORD IDord-6e308a4698204932accf79c9f7fa3056
Source noteuspto-grants-1991_07