子结构搜索

13945

CC(C)CN(C(=O)CCl)c1nc(-c2ccccc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42114
2-chloro-N-(6-(2-chlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12
Reaction #45398
desired product
收率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(/C=C/C(=O)O)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45399
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2csc3c(-c4ccc(O)cc4)cnc(N)c23)cc1
Reaction #45412
desired product
收率 125.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NC(=O)Nc2ccc(-c3csc4c(C#CCCO)cnc(N)c34)cc2)c1
Reaction #45413
desired product
收率 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12
Reaction #45419
desired product
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(/C=C/C(=O)O)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45421
desired product
收率 128.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12)OCC
Reaction #45433
desired product
收率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(/C=C/C=O)c2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45434
desired product
收率 106.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45435
acetate salt
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(N)c(OC)c3)csc12
Reaction #45437
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCc1cnc(N)c2c(-c3ccc(NC(=O)Nc4cccc(C)c4)cc3)csc12
Reaction #45440
desired product
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1Cc2cc(/C=C/C(=O)N(C)Cc3c(C)[nH]c4ccccc34)cnc2NC1=O
Reaction #46626
title compound
收率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc(N)c(/C=C/CCOCc2ccccc2)c1-c1ccc(F)cc1
Reaction #57363
methyl (E)-6-amino-5-(4-(phenylmethoxy)but-1-enyl)-4-(4-fluorophenyl)-2-(1-methylethyl)nicotinate
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57364
mixture
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)C)nc(N)c(C=O)c1-c1ccc(F)cc1
Reaction #57366
ethyl 6-amino-4-(4-fluorophenyl)-5-formyl-2-isopropylnicotinate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc2c(c1-c1ccc(F)cc1)CCCN2
Reaction #57367
methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate
收率 92.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc2c(c1-c1ccc(F)cc1)CCCN2S(C)(=O)=O
Reaction #57368
methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate
收率 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(Cl)cc3Cl)n2)nc1
Reaction #60099
1-{6-[(2-{[4-(2,4-dichlorophenyl)-5-imidazolylpyrimidin-2-yl]amino}ethyl)-amino]-3-pyridyl}ethan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(Cl)cc3Cl)n2)ccc1C#N
Reaction #60108
6-[(2-{[4-(2,4-dichlorophenyl)-5-imidazolylpyrimidin-2-yl]amino}ethyl)amino]-2-methoxypyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
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