8-[(2,5-dichloro-4-pyridinyl)amino]-2-methyl-3,4-dihydroisoquinolin-1-one

CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #118
Ausbeute 42.5%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #119
Ausbeute 63.3%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #120
Ausbeute 49.4%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #121
Ausbeute 59.5%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #219
Ausbeute 48.0%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #220
Ausbeute 43.8%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #221
Ausbeute 26.9%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #222
Ausbeute 30.3%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #223
Ausbeute 69.8%750 AstraZeneca ELN dataset
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #174221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #232891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nn(CCO)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(Cl)cn1
Reaction #387105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN1CCc2cccc(Nc3cc(Nc4cnn(CC(=O)O)c4)ncc3Cl)c2C1=O
Reaction #1133107
2-[4-[[5-chloro-4-[(2-methyl-1-oxo-3,4-dihydroisoquinolin-8-yl)amino]pyridin-2-yl]amino]pyrazol-1-yl]acetic acid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CN1CCc2cccc(Nc3cc(Cl)ncc3Cl)c2C1=O
Reaction #1133108
8-[(2,5-dichloropyridin-4-yl)amino]-2-methyl-3,4-dihydroisoquinolin-1-one
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #1133127
8-(5-chloro-2-(1-methyl-1H-pyrazol-5-ylamino)pyridin-4-ylamino)-2-methyl-3,4-dihydroisoquinolin-1(2H)-one
Ausbeute 69.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1nn(C(F)F)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(Cl)cn1
Reaction #1133149
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1nn(CCO)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(Cl)cn1
Reaction #1133150
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cc1nn(C(F)F)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(Cl)cn1
Reaction #1239828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CN1CCc2cccc(Nc3cc(Nc4cnn(CC(=O)O)c4)ncc3Cl)c2C1=O
Reaction #2433929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)