بحث البنية الفرعية

1174356

CS(=O)(=O)CC(=O)NCCc1nc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)cs1
Reaction #6930
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CC(=O)NCCc1ccc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)o1
Reaction #6931
(4-(3-Fluorobenzyloxy)-3-chlorophenyl)-(6-(5-(2-(methylsulfonyl)acetamidoethyl)-furan-2-yl)-quinazolin-4-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C=Cc1ccc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)o1
Reaction #6934
title compound
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1ccc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)o1)NCCS(=O)(=O)c1ccccc1
Reaction #6935
3-(5-{4-[4-(3-Fluoro-benzyloxy)-3-chloroanilino]-6-quinazolinyl}-2-furyl)-N-[2-(phenylsulfonyl)ethyl]-2-propenamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)CCNC(=O)C=Cc1ccc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)o1
Reaction #6936
title compound
المردود 18.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6937
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)CCNCC1(c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)CC=CO1
Reaction #6939
(4-(3-Fluorobenzyloxy)-3-chlorophenyl)-(6-(2-((2-propanesulphonyl-ethylamino)-methyl)-furan-2-yl)-quinazolin-4-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6940
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OCc2cccc(F)c2)c(Cl)c1
Reaction #66784
title compound
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCc2cccc(F)c2)c(Cl)c1
Reaction #66785
aniline
المردود 120.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1Cc2sc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2C1
Reaction #66806
title compound
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(oc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)C1
Reaction #66844
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2c(sc3ncc(C#N)c(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)C1
Reaction #66846
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C/C=C/C(=O)N1Cc2sc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2C1
Reaction #66864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C/C=C/C(=O)N1CCc2c(oc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)C1
Reaction #66902
title compound
المردود 38.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C)C/C=C/C(=O)N1CCc2c(sc3ncc(C#N)c(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)C1
Reaction #66905
title compound
المردود 61.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCNCc1ccc(-c2ccc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c3c2)o1
Reaction #79428
N-{3-Chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2-(methanesulphonyl)ethyl]amino}methyl)-2-furyl]-4-quinazolinamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1.O
Reaction #155384
p-toluenesulfonic acid monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCc2cccc(F)c2)c(Cl)c1
Reaction #175970
DOI: 10.1039/C8SC04228D
CCOCCn1ccc2ncnc(Nc3ccc(OCc4cccc(F)c4)c(Cl)c3)c21
Reaction #176852
DOI: 10.1039/C8SC04228D
الصفحة 1التالي