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Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water

Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA)...

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Published in:Synthetic communications 2021-05, Vol.51 (10), p.1581-1587
Main Authors: Jia, Jia, Su, Ye, Yu, Hai-Feng, Du, Hai-Tao, Mei, Ze-Min
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cited_by cdi_FETCH-LOGICAL-c338t-64231ef161f4084736019c178f4b858bfad439ae726013a0c943d9fbd44d882e3
cites cdi_FETCH-LOGICAL-c338t-64231ef161f4084736019c178f4b858bfad439ae726013a0c943d9fbd44d882e3
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container_issue 10
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container_title Synthetic communications
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creator Jia, Jia
Su, Ye
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Du, Hai-Tao
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description Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl)indoles had been developed from the cyclocondensation reaction of β-ethyltho-β-indolyl-α, β-unsaturated ketones and hydroxyl -amine hydrochloride. It was found that in the presence of 1 equivalent of 4-dodecylbenzene sulfonic acid (DBSA) in boiling water, β-ethyltho-β-indolyl-α, β-unsaturated ketones efficiently reacted with hydroxylamine hydrochloride to afford 3-(isoxazol-5)-yl)indoles in good yields and with good to excellent regioselectivity. The method features the advantages of eco-friendly process, good yield and regioselevtivity, operational simplicity, broad substrate scope and ease of scale-up.
doi_str_mv 10.1080/00397911.2021.1894339
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ispartof Synthetic communications, 2021-05, Vol.51 (10), p.1581-1587
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language eng
recordid cdi_crossref_primary_10_1080_00397911_2021_1894339
source Taylor and Francis Science and Technology Collection
subjects 3-isoxazolindoles
Aqueous synthesis
hydroxylamine hydro-chloride
Indoles
Ketones
Regioselectivity
Substrates
Sulfonic acid
Synthesis
β-ethylthio-β-indolyl-α
β-unsaturatedketones
title Eco-friendly and regioselective synthesis of 3-(isoxazol-5)-yl) indoles from β -ethylthio- β -indolyl-α, β -unsaturated ketones in water
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