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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030928Generated: October 30, 2026

Sodium Carbonate → 3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine

https://huagongshe.com/reaction/1030928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,6-DibromopyridazineHCID 248852—
Reactant1-[3-[4-(4,5-Dihydro-2-oxazolyl)phenoxy]propyl]piperazineHCID 14989179—
SolventDimethylformamideHCID 6228—
Product3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazineHCID 1498929716.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4.1 parts of 3,6-dibromopyridazine, 4.34 parts of 1-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]piperazine, 6.4 parts of sodium carbonate and 188 parts of N,N-dimethylformamide was stirred overnight at 65° C. The reaction mixture was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98.5:1.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 1.1 parts (16.4%) of 3-bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine; mp. 169.1° C. (comp. 75).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-de90e4f139464101b6de5f793b517a58
Source noteuspto-grants-1992_04