2-bromo-5-phenyl-1,3,4-thiadiazole

CCCCCCCCCCOc1ccc(-c2nnc(-c3ccccc3)s2)c(F)n1
Reaction #174262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1Cc2cc(-c3nnc(-c4ccccc4)s3)ccc2N1
Reaction #675444
5-(5-phenyl-1,3,4-thiadiazol-2-yl)indolin-2-one
Выход 25.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCCCCC1CCC(COc2nnc(Br)s2)CC1
Reaction #1544477
2-bromo-5-(4-pentylcyclohexylmethoxy)-1,3,4-thiadiazole
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CCCCCCCCCCOc1ccc(-c2nnc(-c3ccccc3)s2)c(F)n1
Reaction #1544478
2-(6-decyloxy-2-fluoropyrid-3-yl)-5-phenyl-1,3,4-thiadiazole
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CCCCCCCCc1nnc(-c2ccccc2)s1
Reaction #1544479
2-Octyl-5-phenyl-1,3,4-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CCN(C#CC(C)Nc1nnc(-c2ccccc2)s1)CC.O
Reaction #1621039
2-[(4-diethylamino butyn-2-yl) amino]-5-phenyl-1,3,4-thiadiazole hydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
O=C1O[C@]2(CN3CCC2CC3)CN1c1nnc(-c2ccccc2)s1
Reaction #2196656
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
O=C1OC2(CN3CCC2CC3)CN1c1nnc(-c2ccccc2)s1
Reaction #2222471
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCCCCC1CCC(COc2nnc(Br)s2)CC1
Reaction #2408837
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)