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    Library Synthesis Chemistry

    We have extensive experience in the synthesis of a variety of libraries ranging between 10-30 members to 2000 member libraries. The dedicated library synthesis team and an allied infrastructure with unidirectional flow of job from synthesis, purification, evaporation, dilution and to final QC, makes the process streamlined and robust.

    Our capabilities include synthesizing libraries in both solution and solid phase, starting with the synthesis of scaffolds/building blocks including complex structure involving multi-step synthesis in milligram to kilogram scale with complete characterization in 5-50 mg scale with >90% purity by LCMS/UV/ELSD data for each library in customer preferred format including vials/shallow/deep/well MT plate (???).

    Types of Chemistries Handled

    Spirocyclization using beta-diketones, Suzuki coupling using variety of reagents, Nuceophillic and SNAr type aminations, amidation and esterifcation, acylation, alkylation, urea, carbamate, pyrazole, pyridone, spiroisoxazoline, oxadiazole formation, reductive amination, ether formation for large libraries, peptide libraries and solid phase amindation.

    Reaction Parameter Variability

    Solution phase parallel synthesis at operating temperature range of -20 Degree C to 150 Degree C and in inert atmosphere (when needed).

    24 wellplate to 96 wellplate formats on flat bed and orbital rotary type shakers. Custom designed teflon filtration.

    Purification and Characterization

    Laboratory scale purification through normal/reverse phase Biotage Quad 3 systems, Combiflash systems, ABI Q trap/API 2000/Water’s analytical LCMS, Water’s and Agilent auto purification systems (DAD/Mass detectors), and analytical HPLC/UPLC systems (UV-DAD/ELS) detectors.

    24 wellplate to 86 wellplate formats on flat bed and orbital rotary type shakers. Custom designed teflon filtration.

    Identification of the pure fractions by FIA-MS analysis, purity of fractions established using UPLC and the pure compound further analysed by LCMS.