2-aminothiophenol

ClCc1nc2ccccc2s1
Reaction #4017
2-chloromethylbenzothiazole
Rendimiento 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1Nc2ccccc2SC1c1ccc(F)cc1
Reaction #5938
2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine
Rendimiento 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1c[nH]c(-c2nc3ccccc3s2)c1
Reaction #6526
2-(pyrrol-2-yl)benzothiazole
Rendimiento 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
ClCc1nc2ccccc2o1
Reaction #7182
2-chloromethylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1ccccc1C1CSc2ccccc2N1
Reaction #46134
3-(2-chloro-phenyl)-3,4-dihydro-2H-1,4-benzothiazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1Nc2ccccc2SC1c1ccccc1
Reaction #46135
2-phenyl-4H-1,4-benzothiazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCSc1ccccc1N
Reaction #50170
2-(dodecylthio)aniline
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Nc1ccccc1SCc1ccccc1
Reaction #50171
2-(benzylthio)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)c1nc2ccccc2s1
Reaction #50939
ethyl 2-benzothiazolecarboxylate
Rendimiento 36.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(S)[C@@H](N)C(=O)O
Reaction #54856
D-penicillamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #65125
( I )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCn1c(=O)[nH]c2c(c1=O)Nc1ccccc1S2
Reaction #65128
1,5-dihydro-3-propyl-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione
Rendimiento 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
c1ccc2[nH]ccc2c1
Reaction #78803
compound ( A )
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Nc1n[nH]cc1-c1nc2ccccc2s1
Reaction #85515
title compound
Rendimiento 40.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Oc1cc2c(c3c1CC=CC3)Nc1ccccc1S2
Reaction #93243
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
COC(=O)c1ccccc1CSc1ccccc1N
Reaction #157641
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(COCc2nc3cc(-c4nc5ccccc5s4)ccc3n2-c2ccccc2)cc1
Reaction #161337
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1nc2cc(-c3nc4ccccc4s3)ccc2n1C1CCOCC1
Reaction #161342
title compound
Rendimiento 1.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCc1nc2cc(-c3nc4ccccc4s3)ccc2n1C1CCOCC1
Reaction #161344
title compound
Rendimiento 8.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)OCc1nc2cc(-c3nc4ccccc4s3)ccc2n1C1CCOCC1
Reaction #161346
title compound
Rendimiento 117.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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