子结构搜索

1982

CC1CN(c2ccc(C(F)(F)F)cc2)CCN1C(=O)c1cc(S(C)(=O)=O)ccc1N1CCOCC1
Reaction #61017
title compound
收率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CCSCC2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc(N2CCOCC2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1F
Reaction #61030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Br)ccc1N1CCOCC1)N1CCN(c2ccc(C(F)(F)F)cc2)CC1
Reaction #61039
(5-Bromo-2-morpholin-4-yl-phenyl)-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(NC(=O)CC)ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2F)cc1F
Reaction #64584
title compound
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(C(F)(F)F)c(Cl)cc1[N+](=O)[O-]
Reaction #82059
3-acetamido-6-chloro-4-nitrobenzotrifluoride
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C(F)(F)F)c(Cl)cc1[N+](=O)[O-]
Reaction #82060
3-amino-6-chloro-4-nitrobenzotrifluoride
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(C(F)(F)F)cc1N
Reaction #82061
3,4-diamino-6-chlorobenzotrifluoride
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(C(F)(F)F)c(Cl)cc1[N+](=O)[O-]
Reaction #82647
3-acetamido-6-chloro-4-nitrobenzotrifluoride
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C(F)(F)F)c(Cl)cc1[N+](=O)[O-]
Reaction #82648
3-amino-6-chloro-4-nitrobenzotrifluoride
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(C(F)(F)F)cc1N
Reaction #82649
3,4-diamino-6-chlorobenzotrifluoride
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87630
desired product
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87640
desired product
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87691
desired product
收率 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87786
desired title product
收率 35.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)[C@H]1CCCO1
Reaction #87787
desired title product
收率 28.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)c1ccccc1F
Reaction #87789
pure product
收率 37.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)c1ccno1
Reaction #87790
pure product
收率 39.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)[C@@H]1CCCO1
Reaction #87794
desired product
收率 11.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccnc1C(=O)NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87795
desired title product
收率 22.2%DOI: 10.6084/m9.figshare.5104873.v1
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