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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane | HCID 10440790 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1,3-Bis[4-[4-(4-isopropoxy-3,5-dimethoxyphenyl)benzoyl]-1-piperazinyl]propane dimethanesulfonate | HCID 22676858 | 89.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787653B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-b2589c33429c4d97b208b64b24d5b853 |
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| Source note | uspto-grants-2004_09 |
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