Поиск подструктуры

CN(C)CCS.Cl

C=CCN(C)CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccccc21.O=C(O)C(=O)O
Reaction #5922
4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)CCNCCN1Cc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43239
4-(2-{4-[3-(1,1-Dioxo-1λ6-[1,2,5]thiadiazepan-2-ylmethyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
O=S(c1ccccc1)C1CN(C(c2ccc(Cl)cc2)c2ccc(Cl)cc2)C1
Reaction #46341
1-[bis(4-chlorophenyl)methyl]-3-[(RS)-phenylsulfinyl]azetidine
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCS(=O)(=O)CC2)cc1
Reaction #57810
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)C1Cc2c(-c3ccccc3)cccc2S(=O)C1
Reaction #65939
3-(N-Isopropyl-N-n-propylamino)-5-phenyl-1-oxothiochroman
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](S(=O)(=O)c2ccc(N3CCN4CCC[C@H]4C3)cc2Cl)C1
Reaction #66325
oil
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4nc5c(cc4Cl)SCC(=O)N5C)CC3)c2c1
Reaction #68267
1-(2-(4-((7-chloro-4-methyl-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazin-6-yl)methylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one
Выход 82.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4nc5c(cc4Cl)SCC(=O)N5C)CC3)c2c1.Cl
Reaction #68268
1-(2-(4-((7-chloro-4-methyl-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazin-6-yl)methylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride
Выход 188.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(SCCN(C)Cc2ccccc2)ccnc1CCl
Reaction #80418
4-(2-(N-benzyl-N-methylamino)ethylthio)-2-chloromethyl-3-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(O)C(c3ccccc3Cl)SC3=NCCCCN32)cc1OC
Reaction #95506
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.OC1(c2ccc3c(c2)OCO3)C(c2ccc(Cl)cc2)SC2=NCCCCN21
Reaction #95510
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.OC1(c2ccccc2Cl)C(c2ccccc2Cl)SC2=NCCCCN21
Reaction #95511
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(O)C(c3ccccc3F)SC3=NCCCCN32)cc1OC.Cl
Reaction #95516
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.OC1(c2ccc3c(c2)OCO3)C(c2ccc(F)cc2)SC2=NCCCCN21
Reaction #95517
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1cc(-c2csc(=Nc3ccccc3)n2C)ccc1Cl
Reaction #96024
4-(4-Chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-phenylimino-4-thiazoline
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)c1cc(-c2csc(=Nc3ccccc3Cl)n2C)ccc1Cl
Reaction #96031
4-(4-Chloro-3-dimethylsulfamoylphenyl)-2-(2-chlorophenylimino)-3-methyl-4-thiazoline
DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1cc(Cl)ccc1N=c1scc(-c2ccc(Cl)c(S(=O)(=O)N(C)C)c2)n1C
Reaction #96035
2-(4-Chloro-2-methylphenyl-imino)-4-(4-chloro-3-dimethylsulfamoylphenyl)-3-methyl-4-thiazoline hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1c(Cl)cccc1N=c1scc(-c2ccc(Cl)c(S(=O)(=O)N(C)C)c2)n1C
Reaction #96039
2-(3-Chloro-2-methylphenyl-imino)-4-(4-chloro-3-dimethylsulfamoylphenyl)-3-methyl-4-thiazoline hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccc(N=c2scc(-c3ccc(Cl)c(S(N)(=O)=O)c3)n2C)cc1
Reaction #96053
4-(4-Chloro-3-sulfamoylphenyl)-3-methyl-2-(4-methylphenyl-imino)-4-thiazoline hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Br.CN1C(=Nc2ccccc2)SCC1(O)c1ccc(Cl)c(S(N)(=O)=O)c1
Reaction #96058
4-(4-Chloro-3-sulfamoylphenyl)-3-methyl-2-phenyliminothiazolidin-4-ol hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее