sulfonyl chloride

O=S(=O)(Cl)c1ccc(OCc2ccccc2)cc1
Reaction #1169
4-benzyloxybenzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(Cl)c1ccc(-c2cccnc2)s1
Reaction #2868
title product
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CC(CCCl)Oc2ncc(Cl)cc2C1=O
Reaction #4911
crude material
Ausbeute 6.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NS(=O)(=O)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #7000
2,4-dinitrobenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
ClC1CCn2nc(-c3ccccn3)c(-c3ccnc4cc(Br)ccc34)c21
Reaction #8358
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(Cl)c1c(Cl)sc(Cl)c1Cl
Reaction #8728
solid
Ausbeute 991.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(Cl)sc(Cl)c1S(=O)(=O)Cl
Reaction #8729
oil
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(Cl)c1ccc2c(c1)OCO2
Reaction #8939
(1,3-benzodioxol-5-yl)sulfonyl chloride
Ausbeute 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCc1c(O)c(Cl)cc2c(C(F)(F)F)noc12
Reaction #9342
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc2sc(Cl)nc2c1
Reaction #9669
2-Chloro-5-fluoro-1,3-benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1ccc2sc(Cl)nc2c1
Reaction #9671
2-chloro-5-(trifluoromethyl)benzothiazole
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1ccc2nc(Cl)sc2c1
Reaction #9673
desired product
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc2cc(Cl)c(N)c(Cl)c2o1
Reaction #9962
6-Amino-5,7-Dichloro-2-Methylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc2cc(F)c(N)c(Cl)c2o1
Reaction #9966
6-Amino-7-Chloro-5-Fluoro-2-Methylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(Cl)c1ccc2c(c1)OCO2
Reaction #11345
(1,3-benzodioxol-5-yl)sulfonyl chloride
Ausbeute 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CCCc1c(SC)n(CC(=O)OCC)c2c(Br)cccc12
Reaction #40895
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NCCc1ccc(O)c(Cl)c1
Reaction #43123
4-(2-Amino-ethyl)-2-chloro-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1nccnc1Cl
Reaction #44982
title compound
Ausbeute 47.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@@H]1CCCN1.Cl
Reaction #50023
product
Ausbeute 225.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)[C@@H]1CCC(=O)N1
Reaction #50035
pyroglutamic methyl ester
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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