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. 2016 Apr 28;6(8):1085–1095. doi: 10.7150/thno.13448

Table 1.

Specifications of the reaction conditions applied in the conjugation high yields of the final compound. All reactions were carried out for 16 h. For the coupling of NODAGA triethylamine (TEA) was used instead of DIPEA.

DOTA NOTA DTPA CHX-A''-DPTA PCTA Oxo-DO3A NODAGA CIM
Chelator precursor DOTA-p-nitro-phenol ester NOTA-difluor-phenol ester DTPA-tetra
(t-butyl ester)
CHX-A''-DTPA isothio-cyanate PCTA-isothio-cyanate Oxo-DO3A isothio-cyanate NODAGA isothio-cyanate CIM
Equivalents Chelator 4 2 2 3 2 2 2 2
Equivalents DIPEA 20 10 10 10 16 16 10 (TEA) 10
Equivalents HATU - - 1.96 - - - - 1.90
Purification gradient 10-40% ACN 10-40% ACN 10-40% ACN 20-50% ACN 15-45% ACN 15-45% ACN 15-45% ACN 25-55% ACN