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Sc1ccncc1

diphenylmethyl ester

Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1

O=C(O)c1cccnc1

3-pyridinecarboxylic acid

DOI: 10.6084/m9.figshare.5104873.v1

OCCCSc1ccncc1

desired compound

Ausbeute 83.9%DOI: 10.6084/m9.figshare.5104873.v1

OCCCSc1ccncc1

desired compound

Ausbeute 62.9%DOI: 10.6084/m9.figshare.5104873.v1

O=C1c2ccc([N+](=O)[O-])cc2C(=O)N1CSc1ccncc1

desired compound

Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1

O=C(NCSc1ccncc1)c1cccnc1

desired compound

Ausbeute 15.9%DOI: 10.6084/m9.figshare.5104873.v1

CCC(=O)N(CCCCSc1ccncc1)c1ccccc1N(CCCCSc1ccncc1)C(=O)CC

desired product

Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1

ClCCCCSc1ccncc1

desired compound

Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1

C#CCSc1ccncc1

Reaction #55320

4-(2-propynylthio)pyridine

Ausbeute 40.2%DOI: 10.6084/m9.figshare.5104873.v1

Nc1ccc(Cl)cc1Sc1ccncc1

Reaction #57916

4-chloro-2-(pyridin-4-ylsulfanyl)-phenylamine

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)NC1=NC(CSc2ccncc2)CS1

Reaction #76056

tert-butyl N-[(4RS)-4-(4-pyridylsulphanylmethyl)-4,5-dihydro-2-thiazolyl]carbamate

Ausbeute 28.2%DOI: 10.6084/m9.figshare.5104873.v1

$O=C(CCCSc1ccncc1)NC/C=C\COc1cc(CN2CCCCC2)ccn1$

Reaction #80366

Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #81885

diphenylmethyl ester

Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)Sc1ccncc1

Reaction #189366

DOI: 10.1039/C8SC04228D

CC1(C)SC2C(NC(=O)CSc3ccncc3)C(=O)N2C1c1nnn[nH]1

Reaction #192053

DOI: 10.1039/C8SC04228D

O=[N+]([O-])c1ccc(Sc2ccncc2)c(F)c1

Reaction #211511

DOI: 10.1039/C8SC04228D

Cc1ccc(NC(=O)Nc2ncc(Sc3ccncc3)s2)c(C(=O)C2CCCC2)c1

Reaction #219091

1-(2-Cyclopentanecarbonyl-4-methyl-phenyl)-3-[5-(pyridin-4-ylsulfanyl)-thiazol-2-yl]-urea

Ausbeute 25.1%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #243283

DOI: 10.1039/C8SC04228D

O=C(NCSc1ccncc1)c1cccnc1

Reaction #248347

DOI: 10.1039/C8SC04228D

Reaction #259426

DOI: 10.1039/C8SC04228D

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