#899190

CC(N)C(Oc1cc2cnn(-c3ccc(F)cc3)c2cc1Cl)c1ccc(F)cc1
Reaction #41395
(1RS,2RS)-1-[6-chloro-1-(4-fluorophenyl)indazol-5-yl]oxy-1-(4-fluorophenyl)propan-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(C2CNC(=O)N2C)cc1NC1CC2CCC1C2
Reaction #64749
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1sc(NCc2ccccc2)c(C#N)c1C
Reaction #72633
2-(Benzylamino)-4,5-dimethylthiophene-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1cc(N2CC3CN(C)CC3C2)ccc1[N+](=O)[O-]
Reaction #164561
N-methyl-5-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-2-nitrobenzamide
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)NC(=O)Cn1c(-c2ccccc2)nc2ccc(N3CC4CN(C)CC4C3)cc2c1=O
Reaction #164584
N-isopropyl-2-(6-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl)acetamide
Ausbeute 39.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)c1cn(C[C@H]2CCCO2)/c(=N/C(=O)c2cc(C(F)(F)F)ccc2CN2CCC[C@H]2CO)s1
Reaction #165734
N-[(2Z)-5-tert-butyl-3-[(2R)-tetrahydrofuran-2-ylmethyl]-1,3-thiazol-2(3H)-ylidene]-2-{[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]methyl}-5-(trifluoromethyl)benzamide
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc2c(c1)C(c1c[nH]c3ccccc13)CC2N1CCCCC1
Reaction #173224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #173352
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCNCCCCNC(=O)OC(C)(C)C
Reaction #173650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCCN(C2CCN(C(=O)Nc3ccccc3C(=O)Nc3ccc(Cl)cn3)CC2)CC1
Reaction #173656
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CNC1Cc2ccccc2C1
Reaction #173767
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)Nc1ccc(Cc2nc3c([nH]2)c(=O)n(Cc2ccccc2F)c(=O)n3CC2CC2)cc1
Reaction #173826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(cc1N1CC(C)N(C)C(C)C1)N(C(C)=O)CC2
Reaction #174178
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(CN2CCC(N3C(=O)Nc4ccccc4C3c3cccc(O)c3)CC2)c1
Reaction #174316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cn(CC2CCN(CCO[Si](C)(C)C(C)(C)C)C2)c2ccc(I)cc2c1=O
Reaction #174338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c(c1)CCC(CN)C2
Reaction #174396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(CCCCC1CCN(C(=O)OCc2ccccc2)CC1)NC(C)C(=O)N1CCCC1C(=O)OC(C)(C)C
Reaction #174769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc2ccccc2c1CN1CCC(Nc2nc3ccccc3s2)CC1
Reaction #175389
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CC(NC(=O)C(Cc1c[nH]cn1)NC(CCc1ccccc1)C(=O)O)C(=O)O
Reaction #175608
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(CCCCNS(=O)(=O)c1ccc(CN(Cc2ncc[nH]2)Cc2nccn2C)cc1)C1CCCCC1
Reaction #175733
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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