2-ethylpiperidine

CC#CCOc1cc(N2CCCCC2CC)ncn1
Reaction #42809
4-(2-butynyloxy)-6-(2-ethylpiperidino)pyrimidine
Выход 32.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC1CCCCN1c1ncnc(Cl)c1F
Reaction #42846
4-chloro-6-(2-ethylpiperidino)-5-fluoropyrimidine
Выход 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62506
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N(C(C)=O)N4CCCCC4CC)sc3cc2s1
Reaction #95386
compounds ( a )
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCC1CCCCN1CCCn1c(=O)oc2ccccc21
Reaction #286763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1CCCCN1CCCCn1c(=O)oc2ccccc21
Reaction #301636
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1CCCCN1C(=O)c1cc2ccccc2c(-c2ccccc2)n1
Reaction #399363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC#CCOc1cc(N2CCCCC2CC)ncn1
Reaction #403102
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC1CCCCN1C(=O)c1cc2ccccc2c(-c2ccccc2)n1
Reaction #404795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=C(C(=O)N1CCCCC1CC)c1c(-c2ccccc2)nc2sc(C)nn12
Reaction #413270
N-[β-(2-Methyl-6-phenyl-imidazo[2,1-b]-1,3,4-thiadiazol-5-yl)-propenoyl]-2-ethyl-piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCC1CCCCN1CCC(=O)N1c2ccccc2C(=O)N(C)c2ccccc21.Cl
Reaction #441965
hydrochloride
Выход 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_03
CCC1CCCCN1c1ccc(Br)cc1C=O
Reaction #487942
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCC1CCCCN1C(=O)C=Cc1c(-c2ccccc2)nn2ccccc12
Reaction #574797
1-[3-(2-phenylpyrazolo[1,5 -a]pyridin-3-yl)acryloyl]-2-ethylpiperidine
Выход 47.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CCOC(=O)C(CC(C)C)c1cc(-c2ccc(C(F)(F)F)cc2)cc(N2CCCCC2CC)c1
Reaction #893971
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC1CCCCN1C(=O)c1ccc(C)nc1NCc1ccco1
Reaction #907141
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC1CCCCN1CCn1c(=O)oc2ccccc21
Reaction #914322
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC1CCCCN1CCCCn1c(=O)sc2ccccc21
Reaction #918705
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)C(CC(C)C)c1cc(-c2ccc(C(F)(F)F)cc2)cc(N2CCCCC2CC)c1
Reaction #976869
2-[5-(2-ethyl-piperidin-1-yl)-4′-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCC1CCCCN1C(=O)C=Cc1c(-c2ccccc2)nn2ccccc12
Reaction #1069133
1-[3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acryloyl]-2-ethylpiperidine
Выход 47.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_02
CC#CCOc1cc(N2CCCCC2CC)ncn1
Reaction #1095871
4-(2-butynyloxy)-6-(2-ethylpiperidino)pyrimidine
Выход 32.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
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