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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006237Generated: October 30, 2026

Methanesulfonic Acid → 1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane dimethanesulfonate

https://huagongshe.com/reaction/1006237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propaneHCID 10440790—
SolventIsopropanolHCID 3776—
Product1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane dimethanesulfonateHCID 2267685889.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 5.90 g (7.29 mmol) of 1,3-bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl) benzoyl]-l-piperazinyl]propane in isopropanol (90 mL) was heated to 50° C. and a solution of 1.41 g (14.7 mmol) of methanesulfonic acid in isopropanol (30 mL) was added. t-Butyl methyl ether (30 mL) was added and the mixture was stirred for 5 minutes at 50° C., for 30 minutes at room temperature, then for 30 minutes in an ice bath. Precipitates were collected by filtration and washed with t-butyl methyl ether to afford 6.54 g of 1,3-bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane dimethanesulfonate as a colorless crystalline powder (yield: 90a). mp: 235.5° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787653B2
Source datasetuspto-grants-2004_09
ORD IDord-b2589c33429c4d97b208b64b24d5b853
Source noteuspto-grants-2004_09