HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380576Generated: November 1, 2026
Hydrochloric Acid → HCID 131710748, compound
https://huagongshe.com/reaction/2380576
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Azepine | HCID 6451476 | — |
| Reactant | HCID 70187121 | HCID 70187121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl Acetate | HCID 6584 | — |
| Product | HCID 9803033 | HCID 9803033 | — |
| Product | HCID 131710748 | HCID 131710748 | 563.3% |
Reaction Steps
1,1-Carbonydiimidazole (0.80 g, 4.9 mmol) was added to a solution of 4-[4-(2-methoxyphenyl)piperazin-1-yl]-3-phenylbutanoic acid dihydrochloride (2.00 g, 4.68 mmol) and triethylamine (0.95 g, 9.4 mmol) in dichloromethane (20 ml). After the cessation of gas evolution, a solution of azepine (0.51 g, 5.2 mmol) in dichloromethane (7 ml) was added and stirring continued overnight. The reaction mixture was concentrated under reduced pressure and the crude product chromatographed on silica gel, eluting with ethyl acetate: hexane (5:1) to afford an oil. The oil was dissolved in methyl acetate and acidified with ethereal hydrogen chloride to afford the title compound dihydrochloride hemihydrate as a colourless powder (1.08 g), m.p. 201.5-202.2 (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05369103 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-722ee7a643a94b7080b200194997dec0 |
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| Source note | uspto-grants-1994_11 |
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