HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358777Generated: November 1, 2026
Hydrochloric Acid → 1-(7,8-Dimethoxy2,3-dihydro-1-benzoxepin-4-ylcarbonyl)-2-methoxymethyl4-(3,4,5-trimethoxybenzoyl)piperazine
https://huagongshe.com/reaction/358777
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7,8-Dimethoxy-2,3-dihydro-1-benzoxepine-4-carbonyl chloride | HCID 10468274 | — |
| Reactant | 3-Methoxymethyl-1-(3,4,5-trimethoxybenzoyl)piperazine | HCID 20066593 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(7,8-Dimethoxy2,3-dihydro-1-benzoxepin-4-ylcarbonyl)-2-methoxymethyl4-(3,4,5-trimethoxybenzoyl)piperazine | HCID 21625211 | — |
Reaction Steps
A solution of 7,8-dimethoxy-2,3-dihydro-1-benzoxepine-4-carbonyl chloride (300 mg) in dichloromethane (10 ml) is added dropwise, taking 30 minutes under ice-cooling while stirring, to a mixture of 3-methoxymethyl-1-(3,4,5-trimethoxybenzoyl)piperazine×hydrochloride (400 mg) obtained in Reference Example 6, triethylamine (1 ml) and dichloromethane (30 ml). The reaction mixture is washed with an aqueous solution of citric acid and an aqueous solution of sodium hydrogencarbonate, then dried over magnesium sulfate, followed by concentration. The concentrate is subjected to a silica gel column chromatography (eluent: ethyl acetate-methanol =95:5) to afford 1-(7,8-dimethoxy2,3-dihydro-1-benzoxepin-4-ylcarbonyl) -2-methoxymethyl4-(3,4,5-trimethoxybenzoyl)piperazine (520 mg) as colorless crystals, m.p. 142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997836 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-d1776094d76841359daecf25d73335d5 |
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| Source note | uspto-grants-1991_03 |
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