TFA

COC(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #911
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1c(S(N)(=O)=O)ccn1C
Reaction #913
title compound
수율 79.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(N)(=O)=O)c1Br
Reaction #915
title compound
수율 21.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON=Cc1c(S(N)(=O)=O)ccn1C
Reaction #918
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)S(=O)(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #920
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #922
title compound
수율 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1ccc(-c2cncc(C3CCCCN3)c2)cc1
Reaction #1135
5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(N)CCN(c2nccc(Cl)n2)CC1
Reaction #1252
4-amino-1-(4-chloropyrimidin-2-yl)-4-methylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(N)CCN(c2ccnc(Cl)n2)CC1
Reaction #1253
4-amino-1-(2-chloropyrimidin-4-yl)-4-methylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC(CF)c1ccsc1S(N)(=O)=O
Reaction #1533
pure title compound
수율 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC(CCl)c1ccsc1S(N)(=O)=O
Reaction #1537
pure title compound
수율 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(COc1ccc(CCN)cc1)OCC
Reaction #1624
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)OCc1ccccc1.O=C(O)C(F)(F)F
Reaction #1683
white powder
수율 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(Cl)cc1C(O)c1ccccc1Cl)C(F)(F)F
Reaction #1889
crystal
수율 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1982
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1984
title compound
수율 58.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@H](N)CCc1ccccc1
Reaction #2010
D-Homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CCCCCOc1ccc(Nc2ccncc2)cc1
Reaction #2332
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C(N)CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2345
title compound
수율 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(OCC(=O)O)cc2)cc1
Reaction #2384
4-{2-[6-(4-tert-butylbenzenesulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yl-oxy]ethoxy}phenoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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