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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494654Generated: November 3, 2026

Triethylamine → HCID 86744880, compound

https://huagongshe.com/reaction/1494654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 15087730HCID 15087730—
ReactantHCID 15087743HCID 15087743—
SolventDimethylformamideHCID 6228—
ProductHCID 86744880HCID 8674488022.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3.6 parts of 1-[5,5-bis(4-fluorophenyl)pentyl]-3-methylpiperazine, 3 parts of N-(4-acetyl-2,6-dichlorophenyl)-2-chloroacetamide, 1.9 parts of N,N-diethylethanamine and 45 parts of N,N-dimethyformamide was stirred for 20 hours at 70° C. The reaction mixture was evaporated and the residue was taken up in a mixture of sodium carbonate and water. The product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried in vacuo at 40° C., yielding 1.74 parts (22.8%) of N-(4-acetyl-2,6-dichlorophenyl)-4-[5,5-bis(4-fluoro-phenyl)pentyl]-2-methyl-1-piperazineacetamide dihydrochloride, 2-propanol(1:1), sesquihydrate; mp. 176.3° C. (compound 54).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026853
Source datasetuspto-grants-1991_06
ORD IDord-b364a1271dbb4f0eba072385fd3ba8ab
Source noteuspto-grants-1991_06