propan-2-yl 4-(6-chloro-5-methoxypyrimidin-4-yl)oxypiperidine-1-carboxylate

COc1c(Nc2ccc(-n3cncn3)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #208
収率 48.5%750 AstraZeneca ELN dataset
COc1c(Nc2ccc(S(C)(=O)=O)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #520
収率 78.4%750 AstraZeneca ELN dataset
COc1c(Nc2ccc(S(C)(=O)=O)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #521
収率 50.0%750 AstraZeneca ELN dataset
COc1c(Nc2ccc(Br)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #205032
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(Nc2ccc(C)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #209057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(Nc2ccc(S(C)(=O)=O)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #222646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1c(Nc2cnc(S(C)(=O)=O)cc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #294874
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1c(OC2CCN(C(=O)OC(C)C)CC2)ncnc1N1CCc2cc(S(C)(=O)=O)ccc21
Reaction #535753
4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1c(Oc2ccc(Br)cc2F)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #758683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1c(Nc2c(C)cc(Br)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #771330
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1c(Nc2ccc(C(C)(C)S(C)(=O)=O)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #889342
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COc1c(Nc2cnc(C#N)cc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #904579
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COc1c(Nc2ccc(S(C)(=O)=O)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #1291967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCCSc1ccc(Nc2ncnc(OC3CCN(C(=O)OC(C)C)CC3)c2OC)c(C)n1
Reaction #1307782
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1c(OC2CCN(C(=O)OC(C)C)CC2)ncnc1N1CCc2cc(S(C)(=O)=O)ccc21
Reaction #1628994
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COc1c(Oc2ccc(Br)cc2F)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #1898736
4-[6-(4-bromo-2-fluoro-phenoxy)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
COc1c(Nc2ccc(Br)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #1898744
4-[6-(6-bromo-2-methyl-pyridin-3-ylamino)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
COc1c(Nc2ccc(C)nc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #1898747
4-[6-(2,6-dimethyl-pyridin-3-ylamino)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
Cl
Reaction #1898748
HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
COc1c(Nc2cnc(S(C)(=O)=O)cc2C)ncnc1OC1CCN(C(=O)OC(C)C)CC1
Reaction #1898750
4-[6-(6-methanesulfonyl-4-methyl-pyridin-3-ylamino)-5-methoxy-pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
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