部分構造検索

8368

COC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #4364
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCC[C@@H](O)[C@@H]1CC(=O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #4365
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.Br.O=C(C[C@@H]1NCCC[C@H]1O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #4366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2cc(Cl)sc2c1=O
Reaction #4367
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.Br.O=C(C[C@@H]1NCCC[C@H]1O)Cn1cnc2cc(Cl)sc2c1=O
Reaction #4368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2c(Br)c(Cl)sc2c1=O
Reaction #4369
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2c(Br)c(Cl)sc12
Reaction #4375
title compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCCC(O)C1CC(=O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #279166
DOI: 10.1039/C8SC04228D
C=CCOC(=O)N1CCCC(OC)C1CC(=O)Cn1cnc2cc(Cl)sc2c1=O
Reaction #1287495
DOI: 10.1039/C8SC04228D
COC(=O)N1CCCC(OC)C1CC(=O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #1317318
DOI: 10.1039/C8SC04228D
C=CCOC(=O)N1CCCC(OC)C1CC(=O)Cn1cnc2c(Br)c(Cl)sc2c1=O
Reaction #1317784
DOI: 10.1039/C8SC04228D
COC(=O)N1CCC[C@@H](OC)[C@@H]1CC(=O)Cn1cnc2c(Cl)c(Cl)sc2c1=O
Reaction #2378840
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2cc(Cl)sc12
Reaction #2378845
6-chlorothieno[3,2-d]pyrimidin-4(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2c(Br)c(Cl)sc12
Reaction #2378846
title compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1