子结构搜索

S=C=NCCCl

COC(=O)c1ccc(NC2=NCCS2)cc1Cl
Reaction #52993
2-chloro-4-(2-thiazolinylamino)benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(C(=O)N=CNNC2=NCCS2)nc1Cl
Reaction #56264
3,5-diamino-6-chloro-N-[(2-thiazolinylamino)aminomethylene]-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(C(=O)NNC=NNC2=NCCS2)nc1Cl
Reaction #56265
3,5-diamino-6-chloro-N-{[(2-thiazolinylamino)iminomethyl]-amino}-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2cc(F)c(NC3=NCCS3)cc2n1Cc1ccccc1
Reaction #68428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C1=NC(=O)CS1)c1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #75294
2-[4-(Hexafluoro-2-Hydroxy-2-Propyl)-N-Methylanilino]-2-Thiazolin-4-One
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ncccc1CNC(=S)Nc1cccc(C(F)(F)F)c1C(F)(F)F
Reaction #229455
DOI: 10.1039/C8SC04228D
CSC1=[SH]CC(CO)N1
Reaction #259932
DOI: 10.1039/C8SC04228D
O=C1Cc2ccccc2N1C1=NCCS1
Reaction #282444
DOI: 10.1039/C8SC04228D
C=C(Cl)CNC(=S)SCc1ccccc1
Reaction #284568
DOI: 10.1039/C8SC04228D
Cl.Clc1cccc(CNC2=NCCS2)c1Cl
Reaction #302890
title compound
收率 163.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(CNC2=NCCS2)c1C.Cl
Reaction #302892
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
ClC1(Cl)C=CC=CC1N=C1SCCN1CC1CCC1
Reaction #363536
2-(2,2-dichlorophenylimino)-3-(cyclobutylmethyl)-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NC(=S)N1CCN=C(c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #401103
DOI: 10.1039/C8SC04228D
CC(C)(C#N)c1ccc(-n2c(=O)n(C(=S)NCCCl)c3cnc4ccc(Br)cc4c32)cc1
Reaction #563380
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(N=C=S)C(Cl)(Cl)Cl)c1ccc(Cl)cc1
Reaction #566682
desired product
收率 0.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(NC(=S)Nc1cccnc1)C(Cl)(Cl)Cl)c1ccc(Cl)cc1
Reaction #566683
desired product
收率 52.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NNC2=NCCS2)c1C
Reaction #569864
2-[2-(2,3-dimethylphenyl)-hydrazino]-2-thiazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(COCCNC2=NCCS2)NC(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #630321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ncccc1CNC(=S)Nc1cccc(C(F)(F)F)c1C(F)(F)F
Reaction #732829
1-(2,3-bis(trifluoromethyl)phenyl)-3-(2-fluoropyridin-3-ylmethyl)thiourea
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(COCCNC2=NCCS2)NC(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #739254
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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