部分構造検索

143400

CCOC(=O)c1c2c(c(O)c[n+]1[O-])C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46267
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(OC(C)=O)c(OC(C)=O)c2c1CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46268
Ethyl 3,4-bis(acetyloxy)-6-(3-chloro-4-fluorobenzyl)-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52049
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52050
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
収率 90.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52051
methyl 2-cyclopropyl-4-(4′-fluorophenyl)quinoline-3-carboxylate
収率 85.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52559
4-(4′-fluorophenyl)-2-cyclopropylquinoline-3-carbaldehyde
収率 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #52560
4-(4′-fluorophenyl)-2-cyclopropylquinoline-3-carbaldehyde
収率 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)C)nc(OC)c(CO)c1-c1ccc(F)cc1
Reaction #65195
Ethyl 4-(4-fluorophenyl)-3-hydroxymethyl-6-isopropyl-2-methoxy-pyridine-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cn2ncc3c(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)nc32)cc1
Reaction #70852
4,6-bis(4-fluorophenyl)-1-(4-methylsulfanylbenzyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nc3nn(C4CCNCC4)cc3c(-c3ccc(F)cc3)c2-c2ccncc2)cc1
Reaction #70853
title compound
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(-n2ncc3c(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)nc32)cc1
Reaction #70858
4,6-bis(4-fluorophenyl)-1-(4-methylsulfanylphenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine
収率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc2c(-c3ccc(-c4cccnc4)s3)c(-c3ccncc3)c(-c3ccc(F)cc3)nc2n1
Reaction #70886
desired compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc2c(-c3ccc(F)cc3)c(-c3ccnc(Nc4ccc(S(N)(=O)=O)cc4)c3)c(-c3ccc(F)cc3)nc2n1
Reaction #70888
desired compound
収率 17.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)NCCn2cc3c(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)nc3n2)CC1
Reaction #70896
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccc(F)cc2)c(C2CC2)nc2cc(Br)ccc12
Reaction #174597
DOI: 10.1039/C8SC04228D
C=Cc1c(C(C)C)nc(C(C)C)c(CCCCC)c1-c1ccc(F)cc1
Reaction #175939
DOI: 10.1039/C8SC04228D
CCCCCCc1c(C(C)C)nc(C(C)C)c(C(C)O)c1-c1ccc(F)cc1
Reaction #185451
DOI: 10.1039/C8SC04228D
CCCCCc1c(C(C)C)nc(C(C)C)c(C(O)CCCC)c1-c1ccc(F)cc1
Reaction #185917
DOI: 10.1039/C8SC04228D
Cn1cc2c(-c3ccc(F)cc3)c(-c3ccnc(Nc4ccc(S(N)(=O)=O)cc4)c3)c(-c3ccc(F)cc3)nc2n1
Reaction #186918
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(=O)CC(=O)C=Cc1c(C2CC2)nc2ccccc2c1-c1ccc(F)cc1
Reaction #190852
DOI: 10.1039/C8SC04228D
1 ページ次のページ