1-(2-chloroethyl)pyrrolidine hydrochloride

c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1
Reaction #1176
brown oil
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccc(OCCN2CCCC2)c1[N+](=O)[O-]
Reaction #7045
1-[2-(3-Methyl-2-nitrophenoxy)-ethyl]-pyrrolidine
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cccc(OCCN2CCCC2)c1
Reaction #45919
3-(2-pyrrolidin-1-yl-ethoxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
c1ccc(-c2ccc3nnc(CNc4ccnc5cc(OCCN6CCCC6)cnc45)n3n2)cc1
Reaction #68473
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc2c(c1C=NOCCN1CCCC1)OCO2
Reaction #70964
1-(5-bromo-1,3-benzodioxol-4-yl)-N-[2-(pyrrolidin-1-yl)ethoxy]methanimine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCC(=O)c1ccc(OCCN2CCCC2)cc1Cl
Reaction #94887
1-{2-Chloro-4-[2-(N-pyrrolidinyl)ethoxy]-phenyl}-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Fc1cc2ncccc2cc1Cc1cnc2ccc(-c3cnn(CCN4CCCC4)c3)nn12
Reaction #156435
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(-c2ccc3nnc(CNc4ccnc5cc(OCCN6CCCC6)cnc45)n3n2)cc1
Reaction #306264
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine
Ausbeute 22.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)c1ccc(OCCN2CCCC2)cc1
Reaction #353082
27-6
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Clc1cc(Br)ccc1OCCN1CCCC1
Reaction #358827
1-[2-(4-bromo-2-chloro-phenoxy)-ethyl]-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Brc1ccc2c(c1)CCN2CCN1CCCC1
Reaction #358867
5-bromo-1-(2-pyrrolidin-1-yl-ethyl)-2,3-dihydro-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=[N+]([O-])c1ccc2nn(CCN3CCCC3)cc2c1
Reaction #358881
5-nitro-2-(2-pyrrolidin-1-yl-ethyl)-2H-indazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Brc1cccc(SCCN2CCCC2)c1
Reaction #360696
product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1ccc2c(c1)C=Cc1sc(C)nc1C2c1cn(CCN2CCCC2)c(=O)[nH]c1=O
Reaction #411630
subtitle product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cc1cccc(C)c1OCCN1CCCC1.Cl
Reaction #413848
N-[2-(2,6-dimethylphenoxy)ethyl]pyrrolidine hydrochloride
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
Cc1ccc(C(=O)NC2CC2)cc1-n1ccnc(NCCc2ccc(OCCN3CCCC3)cc2)c1=O
Reaction #424227
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1ccc(C(=O)NC2CC2)cc1-n1ccnc(NC(C)(C)c2ccccc2OCCN2CCCC2)c1=O
Reaction #424229
title compound
Ausbeute 27.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1cccc(C)c1OCCN1CCCC1.Cl
Reaction #432229
N-[2-(2,6-dimethylphenoxy)ethyl]pyrrolidine hydrochloride
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
Cc1ccc2c(c1)c(N1CCN(C(=O)c3cccs3)CC1)c(C#N)c(=O)n2CCN1CCCC1
Reaction #433824
pale yellow solids
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCOC(=O)C1=C(C)NC(CSCCN2CCCC2)=C(C(=O)OCC)C1c1cccc([N+](=O)[O-])c1
Reaction #446171
2-[2-(pyrrolidin-1-yl)ethylthio]methyl-3,5-dicarboethoxy-4-(m-nitrophenyl) -6-methyl-1,4-dihydropyridine
Ausbeute 41.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
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