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NC(N)=S

Cc1nc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)sc1C
Reaction #53344
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NC(=O)CS1)OCO3
Reaction #53346
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1SC(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)=NC1=O
Reaction #53347
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NC(=O)CCS1)OCO3
Reaction #53348
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nncs1)OCO3
Reaction #53350
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)s1
Reaction #53351
title compound
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NN=C(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)SC1
Reaction #53354
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NNC(=O)CS1)OCO3
Reaction #53355
title compound
Ausbeute 37.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)NCCNCc1ncccn1)c1ccccc1
Reaction #55132
N-benzoyl-N'-[2-(2-pyrimidylmethylamino)-ethyl]thiourea
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(S)nc(-c2ccncc2)cc1=O
Reaction #60578
title compound
Ausbeute 72.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc(N2C(=O)N(c3ccc(C#N)c(C(F)(F)F)c3)C(=O)C2(C)C)cc1F
Reaction #67036
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(C(=S)n3ccnc3)C[C@H]2OC)nc1Cl
Reaction #71796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccccc1NC1=NC(=O)C(C(C)C)S1
Reaction #74330
5-isopropyl-2-[(2-isopropylphenyl)amino]-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(Nc2ccccc2C(C)C)=NC1=O
Reaction #74331
5-ethyl-2-[(2-isopropylphenyl)amino]-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](O[C@H]1C[C@H]2C[C@@H]1C[C@@H]2NC(N)=S)(c1ccccc1)c1ccccc1
Reaction #74435
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N(CC)CC)n1
Reaction #80992
desired compound
Ausbeute 140.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)c1ccccc1N1C(=O)CS/C1=N\C(=O)Nc1ccc(-c2ncn(-c3ccc(OC(F)(F)F)cc3)n2)cc1
Reaction #88135
title compound
Ausbeute 102.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)Nc1ccccc1C1CC1
Reaction #88143
1-(2-cyclopropylphenyl)thiourea
Ausbeute 56.7%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(-c2ccc(OC)cc2)c(-c2cccnc2)s1
Reaction #93306
4-(4-methoxyphenyl)-2-methylamino-5-(3-pyridyl)-1,3-thiazole
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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