4.alpha.-Hydroxy-6-oxo-2.beta.-arylmethoxy-methyl-3.alpha.-tetrahydropyranacetic acid .gamma.-lactones

Abstract

The present specification provides novel intermediates and novel processes for the synthesis of Thromboxane B.sub.2 (11a-homo-11a-oxa-PGF.sub.2.alpha.), its 15-epimer, and various carboxyl derivatives thereof. In particular, there are disclosed various bicyclic tetrahydrofuran-containing lactones useful in the above processes, and corresponding acyclic lactones.

Description

The present invention relates to Thromboxane B.sub.2 and associated intermediates and processes, for which the essential material constituting disclosure therefor is incorporated by reference here from Ser. No. 676,890, filed Apr. 14, 1976, now issued as U.S. Pat. No. 4,020,173 on Apr. 26, 1977.

Claims

1. A thromboxane intermediate of the formula ##STR1## wherein R.sub.34 is an arylmethyl hydroxy-hydrogen replacing group selected from the group consisting of

(a) benzyl,

(b) benzyl substituted by one to five alkyl of one to four carbon atoms, inclusive, chloro, bromo, iodo, fluoro, nitro, phenylalkyl of 7 to 12 carbon atoms, inclusive,

(c) benzhydryl,

(d) benzhydryl substituted by one to ten alkyl of one to four carbon atoms, inclusive, chloro, bromo, iodo, fluoro, nitro, phenylalkyl of 7 to 12 carbon atoms, inclusive,

(e) trityl, and

(f) trityl substituted by one to 15 alkyl of one to four carbon atoms, inclusive, chloro, bromo, iodo, fluoro, nitro, phenylalkyl of 7 to 12 carbon atoms, inclusive.

2. 4.alpha.-Hydroxy-6-oxo-2.beta.-benzyloxymethyl-3.alpha.-tetrahydropyranacetic acid .gamma.-lactone, a thromboxane intermediate according to claim 1.