tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate

CC(C)(C)OC(=O)N1CC2CC1CN2Cc1cccc(-c2ccnc(Cl)n2)c1
Reaction #43234
5-[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CC2CC1CN2c1ccc(F)nc1
Reaction #177151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1cncnc1
Reaction #186958
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1nccs1
Reaction #191083
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1nc(-c2ccnc(Cl)c2)cc2nccn12
Reaction #197224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Nc1cc(-n2nc(N3CC4CC3CN4C(=O)OC(C)(C)C)c3ccccc32)ccn1)c1ccccc1
Reaction #198818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2C(=O)c1cccc(Cl)c1Cl
Reaction #202813
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1ccc(-c2ccccc2)nn1
Reaction #212892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CC1CN2
Reaction #227121
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(-c2noc(CN3CC4CC3CN4)n2)cc2c1C(=O)N(Cc1ccc(OC(F)(F)F)cc1)C2
Reaction #228557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1nc2c(cnn2CC)c(NC2CCOCC2)c1CNC(=O)c1cccc(C(=O)NCc2ccc(C#N)c(-c3cccc(CN4CC5CC4CN5)c3)c2)c1
Reaction #235742
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1cccnc1
Reaction #243056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1cncc(Br)c1
Reaction #246677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1noc(N2CC3CC2CN3C(=O)OC(C)(C)C)n1
Reaction #249094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CC2CC1CN2S(C)(=O)=O
Reaction #257271
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCOc1cc(N2CC3CC2CN3C(=O)OC(C)(C)C)cnc1Cl
Reaction #264964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CC2CC1CN2Cc1cccc(-c2ccnc(Cl)n2)c1
Reaction #266110
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1ccc(F)nc1
Reaction #274992
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CC2CC1CN2c1cnc2ccccc2c1
Reaction #278276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(N2CC3CC2CN3C(=O)OC(C)(C)C)sn1
Reaction #280380
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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