Process for the preparation of dibenzothiepin derivative

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

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560 9, 560152, 560153, 562431, C07D33714, C07C14940

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048914339

ABSTRACT:
A novel process for the preparation of 2-(10,11-dihydro-10-oxodibenzo[b, f]thiepin-2-yl)propionic acid which shows high anti-inflammatory and analgetic action is disclosed. The process starts from a propiophenone derivative having the formula (II): ##STR1## wherein R.sup.1 is hydrogen or a lower alkyl group, which is once converted into a haloacetal compound via a halo-ketone compound, and then converted into the desired dibenzothiepin derivative through a combination of rearrangement, hydrolysis and ring closure in variable sequences.

REFERENCES:
patent: 4247706 (1981-01-01), Fujimoto et al.
Patent Abstracts of Japan, vol. 7, No. 213, p. 132.
Patent Abstracts of Japan, vol. 6, No. 197, p. 54.
Streitwieser & Heathcock, Introduction to Organic Chemistry, pp. 766-767.

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