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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780672Generated: October 31, 2026

2-Chlorobenzoxazole → 4-(2-Benzoxazolyl)hexahydro-1H-1,4-diazepine-1-ethanol

https://huagongshe.com/reaction/1780672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant2-(1,4-Diazepan-1-yl)ethan-1-olHCID 2736550—
SolventDimethylformamideHCID 6228—
Product4-(2-Benzoxazolyl)hexahydro-1H-1,4-diazepine-1-ethanolHCID 1904728326.6%

Reaction Steps

A 2.329 g portion of homopiperazine dissolved in 10 ml of THF was mixed with 830 mg of iodoethyl alcohol to carry out 24 hours of reaction at room temperature. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was purified by Sephadex LH-20 (Pharmacia) (chloroform:methanol=1:1) and Diaion HP-20 (Mitsubishi Chemicals) to obtain 305 mg of 1-(2-hydroxyethyl)homo-piperazine. Next, Under cooling with ice, 150 mg of 1-(2-hydroxyethyl)homopiperazine and 159 mg of 2-chlorobenzoxazole were added to 3 ml of DMF, and the reaction was carried out for 17 hours at the same temperature and then for 24 hours at room temperature. The reaction mixture was concentrated under a reduced pressure, and the resulting residue was dissolved in 100 ml of ethyl acetate, washed with sodium hydrogencarbonate aqueous solution (pH 8) and water in that order, dehydrated with sodium sulfate and then concentrated under a reduced pressure. Thereafter, the resulting residue was purified by a silica gel column chromatography (chloroform:methanol=30:1) to obtain 72 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631257
Source datasetuspto-grants-1997_05
ORD IDord-bc5da25555fc4763bd56a9c7721645cd
Source noteuspto-grants-1997_05