butanal

CCCC(c1c[nH]c2ccccc12)c1c[nH]c2ccccc12

1,1-di-indol-3-yl-butane

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCC(c1c[nH]c2ccc([N+](=O)[O-])cc12)c1c[nH]c2ccc([N+](=O)[O-])cc12

1,1-di-(5 nitroindol-3-yl)-butane

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCC(c1c[nH]c2ccc(F)cc12)c1c[nH]c2ccc(F)cc12

1,1-di-(5-fluoroindol-3-yl)-butane

Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCC(c1c[nH]c2ncccc12)c1c[nH]c2ncccc12

1,1-di-(7-azaindol-3-yl)-butane

Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCC(c1ccc[nH]1)c1ccc[nH]1

1,1-di-(2-pyrryl)-butane

Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCCC1Cc2cc(OC)ccc2C1=O

2-butyl-5-methoxy-1-indanone

Ausbeute 104.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCC=C1Cc2cc(OC)ccc2C1=O

2-butylidene-5-methoxy-1-indanone

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCCC1Cc2cc(OC)ccc2C1=O

2-butyl-5-methoxy-1-indanone

Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCCCNCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1

(1H-benzimidazol-2-ylmethyl)-(4-butylaminomethyl-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08

CCC(C=O)=Cc1ccccc1

Reaction #40776

desired product

Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCc1nc2cc(NS(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C

Reaction #43805

crude sub-title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCc1nc2c([N+](=O)[O-])cccc2[nH]1

Reaction #43814

sub-title compound

Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCc1nc2cc(NS(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C

Reaction #43819

crude sub-titled compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCc1nc2cc(NC(=O)OC(C)(C)C)ccc2n1CC(=O)OC(C)(C)C

Reaction #43854

crude sub-title compound

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

$CCCCN(CCCC)Cc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53146

(Z)-3-[1-(4-Dibutylaminomethyl-phenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

$CCCCNCc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53147

(Z)-3-[1-(4-butylaminomethyl-phenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

CCCC=C1CCCCC1N

Reaction #55513

1-BUTYLIDENE CYCLOHEXYLAMINE

Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09

CCCCN1CCN(c2ccc(OC)cc2)CC1.Cl.Cl

Reaction #56004

1-butyl-4-(4-methoxyphenyl)piperazine dihydrochloride

Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09

CCCCOC(=O)CCC

Reaction #56512

Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09

CCCC=O

Reaction #56513

n-butyraldehyde

Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09

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