#8105283

CCC1(C(=O)O)CCN1C(=O)OC(C)(C)C
Reaction #58633
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CC(C(=O)O[C@H]2CC[C@@]3(C)C(C2)C(=O)C[C@@H]2[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]23)C1
Reaction #70406
3β-(N-(tert-Butoxycarbonyl)azetidin-3-ylcarbonyloxy)androstane-6,17-dione
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CC(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4Cl)nc23)C1
Reaction #92291
final product
Ausbeute 61.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #92567
crude product
Ausbeute 127.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CSc1nn(-c2ccccc2)c2cc(NC(=O)C3CN(C(=O)OC(C)(C)C)C3)ccc12
Reaction #155860
tert-butyl 3-((3-(methylthio)-1-phenyl-1H-indazol-6-yl)carbamoyl)azetidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #159585
title compound ( D26 )
Ausbeute 879.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #170233
solid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCC1(C(=O)O)CCN1C(=O)OC(C)(C)C
Reaction #180862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC(C(=O)N2CCC2)C1
Reaction #205302
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)CCCCCC(NC(=O)C1CN(C(=O)OC(C)(C)C)C1)c1nc(Br)cn1COCC[Si](C)(C)C
Reaction #228084
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CC(CO)C1
Reaction #269397
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CC(C(=O)NC(Cc2ccc(Cl)c(Cl)c2)C(=O)N2CCN(c3ccccc3NS(C)(=O)=O)CC2)C1
Reaction #275550
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CC(C(=O)OC2CCC3(C)C(C2)C(=O)CC2C4CCC(=O)C4(C)CCC23)C1
Reaction #293455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #308385
4
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1CC(C(=O)N[C@H](Cc2ccc(Cl)c(Cl)c2)C(=O)N2CCN(c3ccccc3NS(C)(=O)=O)CC2)C1
Reaction #315268
tert-Butyl 3-{N-[(1R)-1-[(3,4-dichlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl]carbamoyl}azetidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)N1CC(C(=O)N[C@H](Cc2ccc(Cl)cc2)C(=O)N2CCN(c3ccccc3N(CC3CC3)S(C)(=O)=O)CC2)C1
Reaction #315282
tert-Butyl 3-{N-[(1R)-1-[(4-Chlorophenyl)methyl]-2-(4-{2-[(cyclopropylmethyl)(methylsulfonyl)amino]phenyl}-piperazinyl)-2-oxoethyl]carbamoyl}-azetidine-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #324478
title compound
Ausbeute 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1CC(CO)C1
Reaction #325654
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)OC(=O)N1CC(CO)C1
Reaction #328820
tert-butyl 3-(hydroxymethyl)azetidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(Oc1ccc(C#N)cn1)C1CN(C(=O)C2CN(C(=O)OC(C)(C)C)C2)CC1c1ccc(Cl)c(Cl)c1
Reaction #391550
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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