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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185824Generated: November 1, 2026

Sodium Carbonate → soluflazine

https://huagongshe.com/reaction/2185824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-N-(2,6-dichlorophenyl)acetamideHCID 77206—
ReactantHCID 22452529HCID 22452529—
SolventDimethylformamideHCID 6228—
ProductsoluflazineHCID 16388532.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-[4-(4-fluorophenyl)-4-(3-pyridinyl)butyl]-2-piperazinecarboxamide (6.75 g), 2-chloro-N-(2,6-dichlorophenyl)acetamide (5.24 g), sodium carbonate (3.16 g) and DMF (143 ml) was stirred for 4 hours at 70° C. The reaction mixture was evaporated and water was added to the residue. After extraction with DCM, the combined organic layers were washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel (eluent:CHCl3/CH3OH 95/5). The desired fractions were collected and the solvent was evaporated. The residue was dissolved in 2-propanol and DIPE and converted into the hydrochloride salt. The salt was filtered off and dried, yielding 2.23 g of 3-(amino-carbonyl)-N-(2,6-dichloro-phenyl)-4-[4-(4-fluorophenyl)-4-(3-pyridinyl)-butyl]-1-piperazineacetamide dihydrochloride.monohydrate (compound 14, mp. 226.3° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403589B1
Source datasetuspto-grants-2002_06
ORD IDord-cd862f798dda42ba83114718b38633d4
Source noteuspto-grants-2002_06