Trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester

CC1=CC(C)(C)Nc2ccc(-c3ccsc3)cc21
Reaction #54074
2,2,4-trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline
Rendimiento 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3F)ccc2N1
Reaction #54076
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccccc3C)cc21
Reaction #54077
4-allylsulfanylmethyl-2,2-dimethyl-6-o-tolyl-1,2-dihydroquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3cccc4c3oc3ccccc34)cc21
Reaction #54078
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccccc3-c3ccccc3)cc21
Reaction #54079
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3-c3ccccc3)ccc2N1
Reaction #54080
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CSc1ccccc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54081
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(OC)c(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)c1
Reaction #54082
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3cccc(OC)c3)cc21
Reaction #54083
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)c1
Reaction #54084
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccc(OC)cc3)cc21
Reaction #54085
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)cc1
Reaction #54086
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccc(OC)c(OC)c3)cc21
Reaction #54087
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)cc1OC
Reaction #54088
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3cc(F)ccc3OC)cc21
Reaction #54089
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(F)cc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54090
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccccc3C(F)(F)F)cc21
Reaction #54091
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3C(F)(F)F)ccc2N1
Reaction #54092
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCSCC1=CC(C)(C)Nc2ccc(-c3cc(C(C)C)ccc3OC)cc21
Reaction #54093
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(C(C)C)cc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54094
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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