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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant4-(4-Chlorophenyl)piperidineHCID 1203613—
Product5-(4-(4-Chlorophenyl)1-piperidinyl)pentyl-2,3,4,5-tetrahydro-1,4-benzoxazepin-3-oneHCID 8674630152.4%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158947
Source datasetuspto-grants-1992_10
ORD IDord-aeb369d7fe5c4430aa0ba780594b2149
Source noteuspto-grants-1992_10