Lactone derivative, process for the preparation thereof, and use

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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549264, 549265, C07D49520, C07D49522, A01N 4322, A61K 31365

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active

045843147

ABSTRACT:
The compound of formula I ##STR1## wherein R.sub.2 is methyl, ethyl, isopropyl or sec-butyl, can be prepared by selective chlorination of an appropriate milbemycin derivative either with hypochlorous acid (HOCl) or sulfuryl chloride (SO.sub.2 Cl.sub.2) in the temperature range from -10.degree. to +60.degree. C. It is employed as pesticide for controlling Arthropode species such as injurious insects or ecto- or endoparasites of animals, and is applied in the form of compositions. This compound is also used as intermediate for obtaining further milbemycin derivatives.

REFERENCES:
patent: 3950360 (1976-04-01), Aoki et al.
patent: 4156720 (1979-05-01), Fisher et al.
Hedge et al., Tetrahedron Letters, vol. 21, pp. 441-444, (1980), "The Reaction of Hypochlorous Acid with Olefins, Convenient Synthesis . . . ".
Hedge et al., Tetrahedron Letters, vol. 22, pp. 5019-5022, No. 5, (1981), "Hypochlorous Acid, Reaction with Conjugated Ketones . . . ".

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