2-chloro-3-nitrothiophene

O=[N+]([O-])c1ccsc1NCCNc1ncc(-c2ncc[nH]2)c(-c2ccc(Cl)cc2Cl)n1
Reaction #60122
[4-(2,4-dichlorophenyl)-5-imidazolylpyrimidin-2-yl]{2-[(3-nitro(2-thienyl))amino]-ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1c(SCCCSc2sccc2[N+](=O)[O-])ccnc1CO
Reaction #173086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)nc(Sc2sccc2[N+](=O)[O-])n1
Reaction #177331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cn(-c2sccc2[N+](=O)[O-])cn1
Reaction #178314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1ccccc1Oc1sccc1[N+](=O)[O-]
Reaction #255454
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccsc1-n1cccn1
Reaction #266116
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccsc1-n1ccnc1
Reaction #407602
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)c1ccccc1Oc1sccc1[N+](=O)[O-]
Reaction #642611
crude desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(C)(C)c1ccccc1Oc1sccc1N
Reaction #763208
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1nc(-c2sccc2[N+](=O)[O-])cn1C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #782362
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc(OC)nc(Sc2sccc2[N+](=O)[O-])n1
Reaction #831164
desired product
المردود 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=[N+]([O-])c1ccsc1-c1cnccn1
Reaction #902526
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1cnn(-c2sccc2[N+](=O)[O-])c1
Reaction #924541
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1cnc(-c2sccc2[N+](=O)[O-])c1
Reaction #1020374
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C1OCCN1c1sccc1[N+](=O)[O-]
Reaction #1023148
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1ccsc1-c1ncco1
Reaction #1029909
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1ccsc1NCCNc1ncc(-c2ncc[nH]2)c(-c2ccc(Cl)cc2Cl)n1
Reaction #1042298
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1ccsc1-c1cscn1
Reaction #1314196
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=[N+]([O-])c1ccsc1-n1cncn1
Reaction #1326932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Nc1ccsc1O[C@@H]1CCOC1
Reaction #1483827
2-[(3R)-tetrahydrofuran-3-yl]oxythiophen-3-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
الصفحة 1التالي