HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833356Generated: October 26, 2026
1-Methylpiperazine → HCID 12828487, compound
https://huagongshe.com/reaction/1833356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | 1-Chloromethyl-5,8-dimethoxyisochroman | HCID 12828439 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12828487 | HCID 12828487 | — |
Reaction Steps
In a sealed tube, 3.0 g of 1-chloromethyl-5,8-dimethoxyisochroman and 6.0 g of N-methylpiperazine were heated at 150°-160° C for 16 hours. After cooling, the reaction mixture was diluted with 200 ml of water and the oily precipitate was extracted with chloroform. The extract was rinsed with water, dried and concentrated under reduced pressure. The residue was chromatographed on a column of silica gel, elution being carried out with a solvent mixture of acetone, benzene and methanol (2:2:1). The oil thus obtained was converted to the fumarate and recrystallized from a solvent mixture of methanol and ether. By this procedure was obtained 1.3 g of 5,8-dimethoxy-1-(4-methylpiperazinyl)methylisochroman fumarate as pale-yellow needles, melting point: 188°-191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04066648 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-5aa7fe9f25fa408a9a496f7f7a78cedb |
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| Source note | uspto-grants-1978_01 |
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