N-(2-chloroethyl)-morpholine

O=Cc1ccccc1OCCN1CCOCC1
Reaction #55243
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OCCN3CCOCC3)ccc21
Reaction #66236
title compound
المردود 10.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc2n(CCCN3CCNCC3)c(=O)c3cnc4[nH]ncc4c3n2n1
Reaction #93986
2-methyl-4-(3-piperazino)propyl-4H-pyrazolo[1,5-a]-pyrazolo[4',3':5,6]pyrido[3,4-e]pyrimidin-5(8H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
—
Reaction #172889
oil
المردود 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)c1ccc(-c2cccn3nc(Nc4ccc(OCCN5CCOCC5)cc4)nc23)cc1
Reaction #174184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)c1ccc(C(CC2CCCC2)C(=O)Nc2ncc(SCCN3CCOCC3)s2)cc1
Reaction #174955
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(OCCN2CCOCC2)c2ccccc12
Reaction #175357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCNCCN1CCOCC1
Reaction #175776
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1ccc(OCCN2CCOCC2)cc1
Reaction #179714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1cc(OCCN2CCOCC2)ccc1F)c1ccc(Nc2ccccc2[N+](=O)[O-])cc1Cl
Reaction #184678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc2n(CCCN3CCNCC3)c(=O)c3cnc4[nH]ncc4c3n2n1
Reaction #186253
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=O)c2ccc3ncccc3c2)cc1NC(=O)c1cccc(OCCN2CCOCC2)c1
Reaction #189622
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Nc2nc(C(O)c3ccc(F)cc3)nc3cc(OC4CCNCC4)ccc23)n[nH]1
Reaction #192827
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1nccn1CCN1CCOCC1
Reaction #193337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1ccccc1OCCN1CCOCC1
Reaction #194366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(OC(C)C)nc(Nc3cc(C)[nH]n3)cc2cc1OCCN1CCOCC1
Reaction #199214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(OCCN2CCOCC2)cc1
Reaction #204730
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1oc2cc(O)ccc2c(OCCN2CCOCC2)c1-c1ccccc1
Reaction #207360
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(-c3cc4c(Cl)ccnc4n3S(=O)(=O)c3ccc(C)cc3)cn(CCN3CCOCC3)c2cc1OC
Reaction #210999
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(C)=O)cc(OC)c1OCCN1CCOCC1
Reaction #211297
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي