HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466966Generated: October 26, 2026
1,4-Dioxane → 5-(4-(4-Chlorophenyl)1-piperidinyl)pentyl-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one
https://huagongshe.com/reaction/466966
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(4-Chlorophenyl)piperidine | HCID 1203613 | — |
| Product | 5-(4-(4-Chlorophenyl)1-piperidinyl)pentyl-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-one | HCID 86746301 | 52.4% |
Reaction Steps
In 10 ml of dioxane was dissolved 65.2 mg of the compound prepared in Reference Example 2, then 123 mg (3 equivalents) of 4-(4-chlorophenyl)piperidine was added thereto, and the resulting mixture was stirred at 110° C. for 6 hours with heating. Thereafter, the same procedures for reaction, treatment and purification as used in Example 1 were repeated to give 46.7 mg (yield: 52.4%) of the title compound. The hydrochloride of this compound was obtained by converting the compound into hydrochloride in the usual manner, and then recrystallizing the salt from methylene chloride-ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158947 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-aeb369d7fe5c4430aa0ba780594b2149 |
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| Source note | uspto-grants-1992_10 |
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