aminopropylmorpholine

Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(NCCCN3CCOCC3)nc21
Reaction #3284
6-(2,6-Dichlorophenyl)-8-methyl-2-(3-morpholin-4-yl-propylamino)-8H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc2nc(NCCCN3CCOCC3)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3538
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #40633
solid
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1=C(C(=O)NCCCN2CCOCC2)C(c2cccc(Cl)c2)NC(=O)N1
Reaction #52882
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(NCCCN1CCOCC1)c1cccc(CS(=O)(=O)C=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)c1
Reaction #53485
3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Brc1cc(-c2nnc(CNCCCN3CCOCC3)o2)c2cn[nH]c2c1
Reaction #67123
title compound
Ausbeute 117.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCCCN1CCOCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67819
3-[(2-fluoro-4-iodophenyl)amino]-N-(3-morpholin-4-ylpropyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCCCN1CCOCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #165984
3-[(2-fluoro-4-iodophenyl)amino]-N-(3-morpholin-4-ylpropyl)isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)C(=C1Nc2ccc(C(=O)NCCCN3CCOCC3)cc2N1)c1nccc(C(F)(F)F)n1
Reaction #180237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1cscc1NC(=O)c1ccc(CNCCCN2CCOCC2)cc1
Reaction #192780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C(=C1Nc2ccc(C(=O)NCCCN3CCOCC3)cc2S1)c1nccc(C(F)(F)F)n1
Reaction #202795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(=O)NCCCN2CCOCC2)ccc1Nc1ncc2c(n1)N(C1CCCC1)CC(F)(F)C(=O)N2C
Reaction #213169
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1ccc(S(=O)(=O)NCCCN2CCOCC2)cc1
Reaction #223753
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCCCN1CCOCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #237896
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ncc(Br)cc1CNCCCN1CCOCC1
Reaction #238475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1cccc(Nc2ncnc3cc(NCCCN4CCOCC4)ccc23)c1
Reaction #238520
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(CN(Cc2ccc(OC)cc2)c2ncc(-c3nc(N4CCOCC4)nc4c3CCN4c3ccc(C(=O)NCCCN4CCOCC4)cc3)cn2)cc1
Reaction #241668
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CC1CSC(c2cc3cc(Cl)cc(NC4CCCC4)c3[nH]2)=N1)NCCCN1CCOCC1
Reaction #248486
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(NCCCN1CCOCC1)C(F)(F)F
Reaction #248581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NC(Cc1ccccc1)C(=O)NCCCN1CCOCC1)c1cc2cc(Cl)ccc2[nH]1
Reaction #249035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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