부분 구조 검색

5831

O=P(O)(O)CCCNCc1ccc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40824
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(CNCCCP(=O)(O)O)nc2-c2ccccc2)cc1
Reaction #40825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(CNCCCP(=O)(O)O)nc2-c2ccncc2)cc1
Reaction #40827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(CNCCCCP(=O)(O)O)nc2-c2ccccc2)cc1
Reaction #40828
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(-c2ccc(CNCCCP(=O)(O)O)nc2-c2ccccc2)cc1
Reaction #40829
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2ccc3c(c2)N(Oc2cccnc2)C(F)(c2cnccn2)N3)cn1
Reaction #41581
2-Fluoropyridin-3-yloxy-6-(6-methanesulfonyl-pyridin-3-yloxy)-2-pyrazin-2-yl-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc([N+](=O)[O-])c(NC)c2)ccn1
Reaction #41763
N-methyl{4-[3-(methylamino)-4-nitro-phenoxy](2-pyridyl))carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2cc([N+](=O)[O-])c(NC)cc2OC)ccn1
Reaction #41770
{4-[2-methoxy-4-(methylamino)-5-nitrophenoxy](2-pyridyl)}-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2cc([N+](=O)[O-])c(NC)cc2OC)ccn1
Reaction #41777
{4-[2-methoxy-4-(methylamino)-5-nitrophenoxy](2-pyridyl)}-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2cc(N)c(NC)cc2OC)ccn1
Reaction #41778
{4-[3-amino-6-methoxy-4-(methylamino)phenoxy](2-pyridyl)}-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(Oc2ccnc(C(=O)NCCO)c2)cc1[N+](=O)[O-]
Reaction #41790
4-(4-Methylamino-3-nitro-phenoxy)-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(Oc2ccnc(C(=O)NCCO)c2)cc1N
Reaction #41791
product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCCCN2CCCC2)cc1N
Reaction #41796
4-(3-Pyrrolidinylpropoxy)benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc(Oc2ccc(N)c([N+](=O)[O-])c2)ccn1
Reaction #41800
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(OC)c(Oc2ccnc(C(N)=O)c2)cc1[N+](=O)[O-]
Reaction #59086
4-(2-methoxy-4-(methylamino)-5-nitrophenoxy)pyridine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC#CCn1c(N2CCC[C@@H](N3C(=O)c4ccccc4C3=O)C2)nc2c1c(=O)n(Cc1ncccc1C#N)c(=O)n2C
Reaction #73183
1-[(3-Cyanopyridin-2-yl)methyl]-3-methyl-7-(2-butin-1-yl)-8-(3-(R)-phthalimidopiperidin-1-yl)-xanthine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(C)CC[C@H](c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)N1
Reaction #156716
title compound
수율 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CC[C@H](c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)N1
Reaction #156717
title compound
수율 97.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1-c1cc([C@H]2CC[C@](C)(C(N)=O)N2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #156726
title compound
수율 65.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1-c1cc([C@H]2CC[C@@](C)(C(N)=O)N2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #156728
title compound
수율 68.3%DOI: 10.6084/m9.figshare.5104873.v1
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