Participa en 50 reacciones

171017

COc1ncc([N+](=O)[O-])cc1-c1ccccc1
Reaction #70260
2-methoxy-5-nitro-3-phenylpyridine
Rendimiento 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1cnc(C2CC2)c(-c2ccccc2)c1
Reaction #70267
2-cyclopropyl-5-nitro-3-phenylpyridine
Rendimiento 17.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cc(C2CC2)ccc1Cl
Reaction #70277
expected product
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(-c2ncc(N)cc2C2CC2)c1
Reaction #70304
5-Cyclopropyl-6-(3-methoxyphenyl)pyridin-3-amine
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)OC[C@H](COc2ccc3c(c2)C(C)(C)c2[nH]c4c(C5CC5)c(C#N)ccc4c2C3=O)O1
Reaction #90129
title compound
Rendimiento 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc(-c2cn3c(n2)-c2ccc(C4CC4)cc2OCC3)n(C(C)CO)n1
Reaction #239444
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)CC1CC(c2onc(C(CCO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)CC(=O)OC(C)(C)C)c2C2CC2)C1
Reaction #245386
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(CC)CC1CC(c2onc(C(CCO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)CC(=O)OC(C)(C)C)c2C2CC2)C1
Reaction #300860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)CC1CC(n2nnc(C(CCO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)CC(=O)OC(C)(C)C)c2C2CC2)C1
Reaction #389677
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1ccc2c(c1)C(C1CC1)=CCO2
Reaction #489980
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CN(C)CCCN(C)c1ccc(C2CC2)cc1[N+](=O)[O-]
Reaction #589922
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CNc1cc(Cl)ncc1C1CC1
Reaction #664082
2-chloro-5-cyclopropyl-N-methylpyridin-4-amine
Rendimiento 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Nc1cnc(C2CC2)cn1
Reaction #683025
5-cyclopropylpyrazin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(C)(C)CC1CC(c2onc(C(CCCOCc3ccccc3)CC(=O)OC(C)(C)C)c2C2CC2)C1
Reaction #750823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)(C)OC(=O)N1CCN2C(=O)c3c(OC(F)(F)F)cc(C4CC4)cc3C2C1
Reaction #905677
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1nc(-c2cn3c(n2)-c2ccc(C4CC4)cc2OCC3)n(C(C)CO)n1
Reaction #973455
270
Rendimiento 27.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC(C)n1nc(N)nc1-c1cn2c(n1)-c1ccc(C3CC3)cc1OCC2
Reaction #973624
431
Rendimiento 23.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COc1cccc(-c2ncc(N)cc2C2CC2)c1
Reaction #1038792
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1(c2ccc(-c3c(-c4ccccc4)oc4c(C5CC5)cccc4c3=O)cc2)CCC1
Reaction #1124464
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CN(C)CCCN(C)c1ccc(C2CC2)cc1[N+](=O)[O-]
Reaction #1129877
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
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