Recherche de Sous-structure

19545

CCNC(=O)Nc1nc2c(s1)C(=O)CCC2
Reaction #9202
4
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)C(=O)C(Br)(Br)CC2
Reaction #9203
compound 5
Rendement 937.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2ccc(Br)c(O)c2s1
Reaction #9204
desired compound 6
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)C(=O)C(Br)CC2
Reaction #9205
desired compound 7
Rendement 166.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2cccc(O)c2s1
Reaction #9206
desired compound 8
Rendement 32.2%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)-c1nc(-c3cccnc3)sc1CC2
Reaction #9247
pure product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)-c1nc(Nc3ccc(Br)cc3)sc1CC2
Reaction #9249
N-[7-(4-Bromoanilino)-4,5-dihydro[1,3]thiazolo[4′,5′: 3,4]benzo[d][1,3]thiazol-2-yl]-N′-ethylurea
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CN(C)CN(c2nc3c(s2)C(=O)CCC3)C1=O
Reaction #9251
pure product
Rendement 100.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)C(Sc1ccccc1)(Sc1ccccc1)CCC2
Reaction #9254
pure product
Rendement 200.4%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2c(s1)C(=O)C(Br)(Br)CC2
Reaction #176556
DOI: 10.1039/C8SC04228D
CN1CC(=O)N(c2nc3c(s2)C(=O)CC(C)(C)C3)C1=O
Reaction #762371
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1nc2c(s1)C(=O)C(Br)CC2
Reaction #781422
DOI: 10.1039/C8SC04228D
CCNC(=O)Nc1nc2c(s1)C(=O)CCC2
Reaction #1204787
DOI: 10.1039/C8SC04228D