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CCN(CC)CCO

CC(=NOCCN1CCOCC1)c1ccccc1
Reaction #10272
acetophenone O-[2-((morpholin-4-yl))ethyl]oxime
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1NC(=O)CCC(=O)O
Reaction #11771
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CN2CCOCC2)c2cccnc12
Reaction #52217
title product
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=O)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52655
3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde
Ausbeute 14.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Cl)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52656
5-chloro-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
Ausbeute 10.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C=C2C(=O)Nc3ccc(Br)cc32)cc(C(C)C)c1OCCN1CCOCC1
Reaction #52688
5-bromo-3-[3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzylidene]-1,3-dihydroindol-2-one
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CNCCN1CCc1ccc2c(c1)OCCO2
Reaction #67962
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(CCn2c(=O)cc(C)c3ccc(OC)cc32)CCN1CCc1ccc2c(c1)OCCO2
Reaction #68084
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)-4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-2-carboxylate
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)sc1C
Reaction #72093
title compound
Ausbeute 7.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #76781
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #77878
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2C(=O)CC[C@H]2C(=O)O)cc1
Reaction #83395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164188
oil
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(C(=O)O[C@H]2CN3CCC2CC3)c2ccccc2)cc1
Reaction #164189
title compound
Ausbeute 54.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN2CCC1CC2CCc1ccccc1
Reaction #176270
DOI: 10.1039/C8SC04228D
Cl
Reaction #179902
DOI: 10.1039/C8SC04228D
COc1ccccc1N1CCN(C(=O)C2CC(N(C)Cc3ccc(F)cc3F)CN2Cc2cccc(Cl)c2)CC1
Reaction #180430
DOI: 10.1039/C8SC04228D
N#Cc1ccc(C(F)(F)F)cc1OCCN1CCOCC1
Reaction #181701
DOI: 10.1039/C8SC04228D
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