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C1CCCC(CC1)N

O=C(CBr)NC1CCCCCC1
Reaction #3058
solid
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1C2CC(O)CC1C1OC12
Reaction #42721
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)N(C2CCCCCC2)C1
Reaction #44477
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1C(=O)C(Cc2ccccn2)C2CCC1C2
Reaction #51411
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)Cc1cc(CNC3CCCCCC3)ccc1-2
Reaction #65917
pale yellow solid
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)ccc1cc(CNC3CCCCCC3)ccc12
Reaction #65918
viscous liquid
Ausbeute 66.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc2c(c1)Cc1ccccc1-2)NC1CCCCCC1
Reaction #65919
N-cycloheptyl-2-fluoreneacetamide
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC1CCCCCC1)c1ccc2c(c1)Cc1ccccc1-2
Reaction #65922
amine
Ausbeute 25.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC23CC4CC(CC2C4)C3)SC12CCC2
Reaction #74320
6-(tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)SC1Cc1c[nH]c2ccccc12
Reaction #74338
2-(cycloheptylamino)-5-(1H-indol-3-ylmethyl)-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC23CC4CC(CC2C4)C3)SC12CCCCC2
Reaction #74349
2-(Tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)OC1c1ccccc1
Reaction #74371
2-(cycloheptylamino)-5-phenyl-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1OC(NC2CCCCCC2)=NC1=O
Reaction #74373
2-(cycloheptylamino)-5-isopropyl-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1OC(NC2CCCCCC2)=NC1=O
Reaction #74374
2-(cycloheptylamino)-5-isobutyl-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2)C(NC2CCCCCC2)c2ccccc21
Reaction #87295
5
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NCc2ccccn2)nc(NC2CCCCCC2)c1C
Reaction #91413
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccc(F)cc2)CC2CCC(C1)N2Cc1ccccc1
Reaction #160016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1CC2CCC(C1)N2CC(C)CN1C(=O)COc2ccc(OC)cc21
Reaction #179362
DOI: 10.1039/C8SC04228D
N#CC1CCCN1C(=O)CNC12CC3CC1CC(O)(C3)C2
Reaction #182201
DOI: 10.1039/C8SC04228D
COc1ccc(Nc2nc(NC3CCCCCC3)nc(OC(C)C)n2)cc1Cl
Reaction #189973
DOI: 10.1039/C8SC04228D
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