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US 4,048,157 AGranted
4(Formylthio)-azetidin-2-ones and ozonization process therefor
AssigneeEli Lilly and Company
InventorsRobin D. G. Cooper, Douglas O. Spry
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Abstract
Ozonolysis of 3-bromomethyl-2-cephem-4-carboxylic acid esters provides 1-(1-protected carboxy-2-hydroxy-3-bromo-1-propenyl)-3-amido(or imido)-4-formylthio-azetidin-2-ones, useful as intermediates in the preparation of cephalosporin antibiotics.
Claims9
A compound of the formula ##STR12## wherein:
- R.sub.1 is a readily removable carboxylic acid protecting group which is substantially unreactive toward ozone;
- and
- R.sub.2 is phthalamido or a group having the formula ##STR13## wherein:
- R.sub.3 is
- 1. hydrogen, C.sub.1 -C.sub.3 alkyl, halomethyl, benzyloxy, 4-nitrobenzyloxy, tert.-butyloxy, 2,2,2-trichloroethoxy, 4-methoxybenzyloxy, 4-protected amino-4-protected carboxybutyl in which the amino protecting group and carboxy protecting group are substantially unreactive toward ozone;
- or
- 2. a group of the formula
- R.sub.4 --(O).sub.m --CH.sub.2 --
- wherein:
- m is 0 or 1;
- and
- R.sub.4 is phenyl or phenyl substituted with 1 or 2 halogens, nitro, cyano, trifluoromethyl, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.2 alkoxy, protected hydroxy in which the hydroxy protecting group is substantially unreactive toward ozone;
- or
- 3. a group of the formula ##STR14## wherein:
- R.sub.4 is as defined above and
- W is protected hydroxy, protected carboxy, or protected amino in which the hydroxy protecting group, the carboxy protecting group and the amino protecting group are substantially unreactive toward ozone.
13 more elements
Dependencies are inferred from the claim text.