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10893

Nc1cc(O)c(C(=O)O)cc1Cl
Reaction #5465
white solid
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(N)cc1O
Reaction #5466
fine colorless needles
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCCOc1cc(N)c(Cl)cc1C(=O)O
Reaction #5472
product
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].[NH4+]
Reaction #72325
ammonium acetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c(C(=O)OCc2ccccc2)c(OC)c1OC
Reaction #76369
product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87551
desired product
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1ccc(F)c(C(F)F)c1
Reaction #87746
desired product
Ausbeute 18.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)F)c1
Reaction #87747
desired product
Ausbeute 26.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1-c1nc(-c2ccc(Cl)cc2)no1
Reaction #87748
desired product
Ausbeute 15.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)(F)F)c1
Reaction #87749
desired product
Ausbeute 22.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(Cl)c(C#N)c(-c3ccc(Oc4ccccc4)cc3)n2)cc1C(=O)O
Reaction #168240
5-(4-chloro-5-cyano-6-(4-phenoxyphenyl)pyridin-2-yl)-2-methoxybenzoic acid
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOc1cccc(C(=O)O)c1OCCCOc1ccc(OCc2ccccc2)cc1
Reaction #178525
DOI: 10.1039/C8SC04228D
COCCOc1ccccc1-c1cn(-c2ccc(C(=O)O)c(O)c2)cc1C#N
Reaction #184457
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCOc1ccc(OCc2ccccc2)c(C(=O)O)c1
Reaction #187668
DOI: 10.1039/C8SC04228D
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)OC)c(OC)cc3OCC(N)=O)cc12
Reaction #188473
DOI: 10.1039/C8SC04228D
Nc1cc(OCc2cccc(Cl)c2)c(C(=O)O)cc1Cl
Reaction #200594
DOI: 10.1039/C8SC04228D
Cc1cc2c(cc1C(F)(F)F)N(Cc1ccc(O)c(C(=O)O)c1)CCCC2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1nnn(C)n1
Reaction #204919
DOI: 10.1039/C8SC04228D
CSCCOc1cc(N)c(Cl)cc1C(=O)O
Reaction #209510
DOI: 10.1039/C8SC04228D
C=CC(=O)OCCCCCCOC(=O)c1cc(OC(=O)c2ccc(OCCCCCCOC(=O)C=C)cc2)ccc1O
Reaction #213750
DOI: 10.1039/C8SC04228D
NCc1c2c(c(I)c(O)c1C(=O)OCc1ccccc1)CCCC2
Reaction #214143
title compound ( 5 )
Ausbeute 108.1%DOI: 10.6084/m9.figshare.5104873.v1
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