مشارك في 201 تفاعل

17677

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Reaction #7578
hydrochloride salt
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
ClCCCN1CCOCC1
Reaction #45265
4-(3-chloropropyl)morpholine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
ClCCCN1CCOCC1
Reaction #51053
3-morpholinopropyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=Cc1ccccc1OCCCN1CCOCC1
Reaction #55240
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Cc1cc(C)nc(N2CCN(c3ccc([N+](=O)[O-])cc3COCCCN3CCOCC3)CC2)c1
Reaction #66143
4-(3-{2-[4-(4,6-dimethyl-pyridin-2-yl)-piperazin-1-yl]-5-nitro-benzyloxy}-propyl)-morpholine
المردود 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CN2C(=O)c3cccc(OCCCN4CCOCC4)c3C2=O)c(OC)c1
Reaction #69690
title compound
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1cc(C(=O)N2Cc3ccc(OCCCN4CCOCC4)cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69699
title compound
المردود 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C(C)c1cc(C(=O)N2Cc3cccc(OCCCN4CCOCC4)c3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69738
(2,4-bis-benzyloxy-5-isopropenyl-phenyl)-[4-(3-morpholin-4-yl-propoxy)-1,3-dihydro-isoindol-2-yl]-methanone
المردود 71.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
ClCCCN1CCOCC1
Reaction #84441
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=[N+]([O-])c1ccc(NCCCN2CCOCC2)c(F)c1
Reaction #84442
title compound
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc2nc(-c3cccc([N+](=O)[O-])c3)nc(Nc3ccc4c(cnn4C(=O)OC(C)(C)C)c3)c2cc1OCCCN1CCOCC1
Reaction #89928
tert-butyl 5-(7-methoxy-6-(3-morpholinopropoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(C=O)c(OCCCN2CCOCC2)c1
Reaction #173476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc(SCCCN2CCOCC2)cc1
Reaction #194852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1SC(=O)N(CCCN2CCOCC2)N=C1c1ccc(OCF)c(OC)c1
Reaction #205809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C=O)c1OCCCN1CCOCC1
Reaction #207783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1ccc(Oc2ccc3c(c2)CCCN(CCCN2CCOCC2)C3)nc1
Reaction #218101
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1CCC(N(C(=O)Nc2ncc(SCCCN3CCOCC3)s2)C2CCCCC2)CC1
Reaction #242778
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2c(=O)n(COC(=O)C(C)(C)C)cnc2cc1OCCCN1CCOCC1
Reaction #255855
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CN=C(c2ccccc2Cl)c2cc(Br)c(OCCCN3CCOCC3)cc2N1
Reaction #260094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2c(Oc3ccc4[nH]cc(C)c4c3)ncnc2cc1OCCCN1CCOCC1
Reaction #272125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي