Substructure Search

Clc1ncccn1

COc1cc(C=O)ccc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #110
Yield 34.9%
COc1cc(OC2CNC2)ccc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #160
Yield 0.0%
Clc1nccc(N2CCCc3ccccc32)n1
Reaction #171
Yield 7.3%
COc1cc(N2CCN(C(C)=O)CC2)c(OC)cc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #209
Yield 0.0%
COc1cc(N(C)CC(=O)OC(C)(C)C)ccc1Nc1ncc(Cl)c(-c2cnc3c(F)cccn23)n1
Reaction #257
Yield 43.0%
NS(=O)(=O)c1cccc(Nc2nccc(Cl)n2)c1
Reaction #333
Yield 2.0%
COc1cc(Nc2ncccn2)ccc1-n1cnc(C)c1
Reaction #353
Yield 18.8%
COc1cccc(Oc2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCNc2ncccn2)c1.O
Reaction #2364
4-tert-butyl-N-[5-(3-methoxyphenoxy)-6-{2-(2-pyrimidinylamino)ethoxy}-pyrimidin-4-yl]benzenesulfonamide hydrate
Yield 161.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(Oc2c(NCCOc3ncccn3)ncnc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1
Reaction #2365
4-tert-butyl-N-[5-(3-methoxyphenoxy)-6-{2-(pyrimidin-2-yloxy)ethylamino}pyrimidin-4-yl]benzenesulfonamide
Yield 92.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ncc(OCc2ccsc2)cn1
Reaction #2418
2-chloro-5-(3-thienylmethoxy)pyrimidine
Yield 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCc1cnc(-c2ccc3c(c2)CC(CCCCCCCC)O3)nc1
Reaction #3161
5-(5-decylpyrimidine-2-yl)-2-octylcoumaran
Yield 23.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2ncc(Cl)cn2)c(Cl)c1
Reaction #4610
3-chloro-4-(5-chloro-2-pyrimidinyloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(C)c1nccc(Cl)n1
Reaction #7728
Ethyl N-(4-chloro-2-pyrimidinyl)-N-methylglycinate
DOI: 10.6084/m9.figshare.5104873.v1
OCCNc1nc(-c2ccco2)c2cnn(CCc3ccccc3)c2n1
Reaction #8398
title compound
Yield 57.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)CCc3ccccc3)ncnc2OCCOc2ncccn2)cc1
Reaction #8712
2-phenyl-ethanesulfonic acid {6-[2-(pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide
Yield 74.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1Oc1c(NS(=O)(=O)Nc2ccc(C(C)C)cc2)nc(-c2ccncc2)nc1OCCOc1ncccn1
Reaction #10347
4-i-propyl-phenyl sulfamic acid-[6-[2-(pyrimidin-2-yloxy)-ethoxy]-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1Cn1ccc2c(-c3ccco3)nc(Cl)nc21
Reaction #11848
title compound
Yield 76.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2nc(-c3ccco3)c3ccn(Cc4ccccc4F)c3n2)cc1OC
Reaction #11849
title compound
Yield 88.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Oc2ccnc(Cl)n2)c(C)cc1N
Reaction #40360
4-(2-chloro-pyrimidin-4-yloxy)-2.5-dimethyl-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Oc2cc(C)c(N)cc2C)nc(Cl)n1
Reaction #40365
4-[(2-chloro-6-methylpyrimidin-4-yl)oxy]-2,5-dimethylaniline
DOI: 10.6084/m9.figshare.5104873.v1
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