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1185100

COc1cc(OC)nc(Nc2ncccc2C(=O)OCc2ccccc2)n1
Reaction #208395
DOI: 10.1039/C8SC04228D
O=C1OC(OC(=O)c2cccnc2Nc2cccc(C(F)(F)F)c2)c2ccccc21
Reaction #214541
phthalidyl 2-(3-trifluoromethylanilino)-3-pyridinecarboxylate
Ausbeute 82.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(F)ccc1C(=O)O
Reaction #938460
desired acid
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)c1nc(OCc2ccccc2)ccc1C(=O)O
Reaction #1210746
DOI: 10.1039/C8SC04228D
Nc1nc(F)ccc1C(=O)O
Reaction #1229895
DOI: 10.1039/C8SC04228D
CCCN(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)c1nc(OCc2ccccc2)ccc1C(=O)O
Reaction #1742785
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Nc2ncccc2C(=O)OCc2ccccc2)n1
Reaction #1857263
yellow-brownish powder
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(OC(=O)c2cccnc2Nc2cccc(C(F)(F)F)c2)c2ccccc21
Reaction #1950390
phthalidyl 2-(3'-trifluormethylanilino)-pyridin-3-carboxylate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(OC(=O)c2cccnc2Nc2cccc(C(F)(F)F)c2)c2ccccc21
Reaction #2421152
DOI: 10.1039/C8SC04228D