Abstract
A few solid phase and solution approaches of good repute were applied in parallel with the aim to provide optimized routes to Boc‐ and Fmoc‐tocinoic acid (3a and 3c) and the corresponding Tyr(Bu^t^) derivatives (3b and 3d). Boc‐tocinoic acid is known to couple with tripeptide amides to give substituted oxytocin precursors in high yields, requiring only Boc‐cleavage to furnish the corresponding hormone analogs with minimal loss of material. For comparison, two protected linear hexapeptides (2a and 2b) were prepared on three polystyrene supports, two with acid‐labile handles and one a conventional chloromethylated resin, in yields of 62–82 and 58–76%, respectively. The intermediate 2a could be converted to 3a with physical data in agreement with those earlier reported. Similarly, the intermediate 2b was converted to 3b. The highest yields for both 2a and 2b were obtained with a 2‐chlorotrityl chloride resin, which in addition provided advantages with respect to overall speed and convenience. Additional syntheses of 3c and 3d on this and of 3c on SASRIN resin, in conjunction with trityl instead of benzyl for side‐chain protection of cysteine, were also elaborated. Copyright © 2001 European Peptide Society and John Wiley & Sons, Ltd.