2-acetylthiazole

c1cnc2nc(-c3nccs3)ccc2c1
Reaction #927
desired product
收率 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CC(=O)c1nccs1
Reaction #67988
methyl 3-oxo-3-(1,3-thiazol-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1cc(-c2nccs2)[nH]n1
Reaction #73100
2-(1H-pyrazol-5-yl)thiazole
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(NCCCCNC(=O)OC(C)(C)C)c1nccs1
Reaction #182772
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=O)CC(=O)c1nccs1
Reaction #217017
2,4-diketo-4-(thiazol-2-yl)butyric acid ethyl ester
收率 72.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(NCCCCNC(=O)OC(C)(C)C)c1nccs1
Reaction #338195
[4-(1-thiazol-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1nc(C)c(-c2ccc3cc(CCN4CCC[C@H]4C)ccc3n2)cc1C(N)=O
Reaction #360421
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCOC(=O)C(=O)CC(=O)c1nccs1
Reaction #373925
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nc(C)c(-c2ccc3cc(CCN4CCCC4C)ccc3n2)cc1C(N)=O
Reaction #392967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nc(C)c(-c2ccc3cc(CCN4CCC[C@H]4C)ccc3n2)cc1C(N)=O
Reaction #638742
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
O=C(CBr)c1nccs1
Reaction #676209
2-bromo-1-(1,3-thiazol-2-yl)ethanone
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1nc(C)c(-c2ccc3cc(CCN4CCC[C@H]4C)ccc3n2)cc1C(N)=O
Reaction #948072
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_12
COC(C)(OC)c1nccs1
Reaction #964545
2-(1,1-dimethoxyethyl)-1,3-thiazole
收率 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
—
Reaction #1094456
solid
收率 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
CC(Nc1cccc2nc(Nc3cccc4c3OC(C)(C)C4)ccc12)c1nccs1
Reaction #1257390
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
COC(C)(OC)c1nccs1
Reaction #1265388
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
CC(O)(c1nccs1)c1nccs1
Reaction #1464737
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
CC(O)(c1nccs1)c1nccs1
Reaction #1543515
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CC(=NO)c1nccs1
Reaction #1635499
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(=NO)c1nccs1
Reaction #1904566
title compound
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
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