The proposed program relates to the development of a universal one-step approach to 1-carbon-2-amino labeling with any isotope of carbon or nitrogen including stable (13C, 15N), radio (14C), and positron-emitting nuclides (11C, 13N). Given the increased involvement of amino acid technology in cancer research and treatment, this proposal is pertinent to the NCI's solicitation for """"""""development and evaluation of special materials for use in medical imaging"""""""" and also to the more general objectives of the DRR. THe advantages of the approach include conservation of isotope (cost savings) and speed in synthesis, the latter attribute being extremely important in routine use of positron-emitting nuclides. The major objective of the program is to investigate the application of cobalt octacarbonyl catalyzed carbonylation of aliphatic aldehydes in the presence of acetamide to give d1-N-acetylamino acids in one step. Secondary objectives include demonstration of 60 percent reaction yield, increased product purity, shortened reaction time, starting-material recovery for recycling isotope, and reaction scale-up capability. The major advantages of the approach are its inherent speed in synthesis, high yield and general applicability. The program approach is to demonstrate the reaction sequence by the preparation of d1-N-acetyl leucine (13C-labeled and unlabeled) and its enzymatically resolved L-amino acid. Demonstration of a cost-effective rapid synthesis of L-amino acids is expected. The reaction investigated, called carbonylacetamidation, should prove superior to the conventional Strecker synthesis in yield and product purity, a special advantage to users of high-cost isotope and short half-life positron emitters. Additionally, the basic reaction scheme is flexible enough to accommodate milligram up to multikilogram unit scales of operation. Immediate applications of the synthesis are in preparation of positron-emitter labeled materials for emission tomography and of stable isotope-labeled materials for clinical research and diagnostic protocol validation.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
5R44CA036666-03
Application #
3506375
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1983-09-30
Project End
1986-09-29
Budget Start
1985-09-30
Budget End
1986-09-29
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Tracer Technologies, Inc.
Department
Type
DUNS #
City
Somerville
State
MA
Country
United States
Zip Code