butan-2-ol

CCC(C)O[Si](OC)(OC)C1CCCC1
Reaction #6541
sec-butoxy cyclopentyl dimethoxysilane
Ausbeute 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(NC(=O)c2cccc(C(F)(F)F)c2)cc1Nc1nccn1-c1cc(Cl)ncn1
Reaction #47773
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(C)[O-].CCC(C)[O-].CCC(C)[O-].[Al+3]
Reaction #50888
Aluminum sec-butoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCC(C)[O-].CCC(C)[O-].CCC(C)[O-].[Al+3]
Reaction #50889
Aluminum sec-butoxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCC(C)OC(=N)N1Cc2ccccc2-c2ccccc2C1
Reaction #63443
2-butyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-carboximidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COc1cnc2c(NCc3nnc4ccc(-c5cc(C)ns5)nn34)ccnc2c1
Reaction #68459
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cnc2c(NCc3nnc4ccc(-c5cc(C)no5)nn34)ccnc2c1
Reaction #68485
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc(-c2ccc3nnc(CNc4ncnc5nc[nH]c45)n3n2)cc1
Reaction #68492
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7H-purin-6-amine
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cnc2c(NCc3nnc4ccc(-c5ccc(N6CCCC6=O)c(F)c5)nn34)ccnc2c1
Reaction #68499
1-(2-fluoro-4-(3-((7-methoxy-1,5-naphthyridin-4-ylamino)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)phenyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(-c2ccc(NN)nn2)sn1
Reaction #68664
1-(6-(3-methylisothiazol-5-yl)pyridazin-3-yl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(C)Oc1c(F)c(F)c(C#N)c(F)c1C#N
Reaction #93736
desired compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Nc1nccn2c(C3CCCCC3)nc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #177058
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1nccc(-c2cccnc2Oc2ccc(Nc3nnc(-c4ccccc4)c4ccccc34)cc2)n1
Reaction #179366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cc(-n2nc3ccc(Cl)cc3n2)c(O)c(C(C)(C)C)c1
Reaction #188742
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)OCc1c(O)ccc2c1CCCC2=O
Reaction #199126
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCO[Si](OCC)(OC(C)CC)C1CCCC1
Reaction #200942
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(O)CC(c2nc(Br)c3c(N)nccn23)C1
Reaction #205699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)O
Reaction #206322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)Oc1nc(Oc2cccnc2)c(-c2ccc(Cl)cc2)c(-c2ccc(Cl)cc2Cl)n1
Reaction #222439
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(=O)OCOC(=O)OC(C)CC
Reaction #230398
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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