306775-46-2

Upstream product

• 50-00-0 formaldehyd 
• 306775-45-1 (S)-N^α-phthaloyl-O-benzyltyrosinylglycine 
• 88036-14-0 (S)-N^α-phthaloyl-O-benzyltyrosine chloride 
• 446256-00-4 [3-(4-benzyloxy-phenyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionylamino]-acetic acid tert-butyl ester 

Downstream Products

• 306775-48-4 4(S)-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1,3,4,5-tetrahydro-80hydroxy-3-oxo-2Hbenzazepin-2-acetic acid 

Relevant academic research and scientific papers

Synthesis of a conformationally constrained tyrosine-glycine dipeptide mimetic: Design of a potential substrate of Syk kinase

The synthesis of a conformationally restricted tyrosine-glycine dipeptide mimetic and its insertion into an octapeptide is described.

Efficient synthesis of (S)-4-phthalimido-1,3,4,5-tetrahydro-8-(2,6-dichlorobenzyloxy)-3-oxo-2H-2-ben zazepin-2-acetic acid (Pht-Hba(2,6,Cl2-Bn)-Gly-OH)

4-Amino-2-benzazepin-3-ones have proven very useful for studying the biologically active conformations of peptides. The synthesis of Pht-Aba-Xaa-OH by reaction of the corresponding 1,3-oxazolidin-5-one with trifluoromethanesulfonic acid (TFMSA) has been reported in the literature. However, when this procedure was applied to the preparation of Pht-Hba(Bn)-Gly-OH 8, many byproducts were formed and the yield of the desired aminobenzazepinones 7 and 8 was very low. We report in this paper an efficient methodology for the synthesis of Pht-Hba(2,6-Cl2-Bn)-Gly-OH 17 starting from the commercially available tyrosine. In our procedure, the dipeptide Pht-Tyr(2,6-Cl2-Bn)-Gly-OH 15 is converted to the 1,3-oxazolidin-5-one 16 which then undergoes Friedel-Crafts cyclization in the presence of tin tetrachloride to afford the desired 4-phthalimido-1,3,4,5-tetrahydro-8-(2,6-dichlorobenzyloxy)-2-benzazepin-3-one 17 in excellent yield.