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391725

CCCCOC=CCNc1ccccc1
Reaction #263753
DOI: 10.1039/C8SC04228D
CCCCOC=CC(=O)N(c1ccccc1)C1CCN(Cc2ccccc2)CC1
Reaction #353956
N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC=CC(=O)N(c1ccccc1)C1CCN(Cc2ccccc2)CC1
Reaction #570664
N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)-aniline
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC1=CC(Nc2ccc(N(CC)C(C)C)cc2)C(N)=CC1=N.Cl
Reaction #674281
4-butoxy-6-[4-(ethylisopropylamino)phenylamino]-3-iminocyclohexa-1,4-dienylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1OC(=C2C(=O)Nc3ccc(F)cc32)c2cnc(Cl)c(Cl)c21
Reaction #1033241
DOI: 10.1039/C8SC04228D
CCCC1OC(=C2C(=O)Nc3ccc(F)cc32)c2cnc(NCCN3CCOCC3)c(Cl)c21
Reaction #1098581
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1OC(=C2C(=O)Nc3ccc(F)cc32)c2cnc(Cl)c(Cl)c21
Reaction #1098582
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCO/C=C\CNc1ccccc1
Reaction #1127500
8e
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC=CC(=O)N(c1ccccc1)C1CCN(Cc2ccccc2)CC1
Reaction #1203305
DOI: 10.1039/C8SC04228D
CCCC1OC(=C2C(=O)Nc3ccc(F)cc32)c2cnc(NCCN3CCOCC3)c(Cl)c21
Reaction #1341313
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1OC(=C2C(=O)Nc3ccc(F)cc32)c2cnc(Cl)c(Cl)c21
Reaction #1341314
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC=CC(=O)N(c1ccccc1)C1CCN(Cc2ccccc2)CC1
Reaction #1735720
N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCO/C=C\CNc1ccccc1
Reaction #1996680
8e
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1