2-methylthiazole

Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #68541
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC(=Cc1nccs1)c1ccc(Cl)cc1
Reaction #211025
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #306338
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc([N+](=O)[O-])ccc1-c1cnc(C)s1
Reaction #369679
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cc1nccs1)c1ccccc1
Reaction #488318
Intermediate 3
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
N/C(=C\c1nccs1)c1ccc(Cl)cc1
Reaction #510287
(Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Oc1ccccc1C=Cc1nc2ccccc2s1
Reaction #547778
title compound
المردود 39.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc(C)s1
Reaction #603319
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CNC(=O)c1c(-c2cnc(C)s2)oc2cc(N(C)S(C)(=O)=O)c(Br)cc12
Reaction #682853
5-bromo-N-methyl-6-(N-methylmethylsulfonamido)-2-(2-methylthiazol-5-yl)benzofuran-3-carboxamide
المردود 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc(C)s1
Reaction #798780
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc(C)s1
Reaction #805352
2-methyl-5-(tributylstannyl)thiazole
المردود 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc(C)s1
Reaction #900309
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOC(=O)C(C)(O)c1cnc(C)s1
Reaction #1010651
ethyl 2-hydroxy-2-(2-methyl-1,3-thiazol-5-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(Cc1nccs1)c1ccccc1
Reaction #1012107
Intermediate 3
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(O)c1cccc(C(=O)O)c1
Reaction #1034772
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #1222502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #1312457
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #1598532
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
Cc1nc[c]([Sn]([CH3])([CH3])[CH3])s1
Reaction #1600904
2-methyl-5-(trimethylstannyl)thiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1.Cc1scc[n+]1N
Reaction #1617223
title compound
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
الصفحة 1التالي