4-(2-chloroethyl)morpholine hydrochloride

C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CCN2CCOCC2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O.O=CO
Reaction #7420
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=NOCCN1CCOCC1)c1ccccc1
Reaction #10272
acetophenone O-[2-((morpholin-4-yl))ethyl]oxime
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cc(OCCC2CNCCO2)c2ccsc2c1
Reaction #11523
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1ccc(Cl)nn1CCN1CCOCC1
Reaction #56678
6-chloro-2-(2-morpholin-4-yl-ethyl)-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(CCN2CCOCC2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O.O=CO
Reaction #61717
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)/C=C/c1ccc(-c2ccc(OCCN3CCOCC3)c(C34CC5CC(CC(C5)C3)C4)c2)cc1
Reaction #70007
(E)-3-[3′-adamantan-1-yl-4′-(2-morpholin-4-yl-ethoxy)biphenyl-4-yl]-acrylic acid methyl ester
Выход 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)N=CC2=C3N=C(Cc4ccccc4)N=C3C(=O)C(CCN3CCOCC3)C2C1=O.Cl.Cl
Reaction #75393
7,7-Dimethyl-2-benzyl-5-(2-morpholino-ethyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Fc1ccc2c(C3CCN(CCN4CCOCC4)CC3)noc2c1
Reaction #83915
N-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]morpholine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCCCCCCCCCCOc1ccc(C(=O)OCCN2CCOCC2)o1
Reaction #85499
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1sccc1S(=O)(=O)N(C)CCN1CCOCC1
Reaction #88021
methyl 3-(N-methyl-N-(2-morpholinoethyl)sulfamoyl)thiophene-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1sccc1N(CCN1CCOCC1)S(C)(=O)=O
Reaction #88023
methyl 3-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)c1ccc(N(CCN2CCOCC2)S(C)(=O)=O)s1
Reaction #88027
tert-butyl 5-(N-(2-morpholinoethyl)methylsulfonamido)-thiophene-2-carboxylate
Выход 119.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #88033
methyl ester
Выход 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCC(=O)c1ccc(OCCN2CCOCC2)cc1Cl
Reaction #94891
1-[2-Chloro-4-(2-morpholinoethoxy)phenyl]-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(CCN3CCOCC3)c12
Reaction #155337
5-fluoro-3-(4-methoxyphenyl)-1-(2-morpholin-4-ylethyl)-8-propoxy-1H-quinolin-4-one
Выход 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1cc2ncccc2cc1Cc1cnc2ccc(-c3cnn(CCN4CCOCC4)c3)nn12
Reaction #156436
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1ccc(-c2cn3c(n2)sc2cc(OCCN4CCOCC4)ccc23)cc1
Reaction #158204
7-(2-morpholin-4-yl-ethoxy)-2-(4-nitrophenyl)imidazo[2,1-b][1,3]benzothiazole
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cn(CCN2CCOCC2)c(=N)s1
Reaction #165720
title compound
Выход 88.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1cc(OCCN2CCOCC2)ccc1Br
Reaction #172350
2-bromo-5-(2-morpholinoethoxy)benzaldehyde
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #172832
solid
Выход 49.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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