N-ethyl-N-(trifluoro-lambda4-sulfanyl)ethanamine

C#CCOc1cc(-n2nc3n(c2=O)CC(F)CC3)c(Cl)cc1Cl
Reaction #2060
title product
Выход 37.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCOc1cc(-n2nc3n(c2=O)CCCC3F)c(Cl)cc1Cl
Reaction #2063
title product
Выход 90.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(CC1CN(CC(F)c2ccc(F)cc2F)C1)c1ccc(F)cc1
Reaction #10316
title compound
Выход 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CF)nc3N21
Reaction #12041
desired compound
Выход 51.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(F)C1CCCN1c1cc2nc(-c3ccccn3)[nH]c2cc1Oc1ccc(S(C)(=O)=O)cc1
Reaction #41642
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
FC(c1cccc(Br)n1)(c1cccc(Br)n1)c1cccc(Br)n1
Reaction #41915
Tris(2-bromo-6-pyridyl)fluoromethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC[C@H]1CF
Reaction #43348
title compound
Выход 12.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NC1CCN(CC2(F)Cn3c(=O)ccc4ncc(F)c2c43)CC1
Reaction #43442
product
Выход 33.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(F)c2oc(C(C)(C)F)nc2c1C#N
Reaction #45881
compound
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
FC1(c2ccc(Br)cc2)CCC1
Reaction #48045
1-bromo-4-(1-fluoro-cyclobutyl)-benzene
Выход 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)C(=O)n1cc(CF)c(S(=O)(=O)c2cccc(Cl)c2C)n1
Reaction #49885
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(-c2ccc(C(F)(F)CCC(=O)O)cc2)cc1
Reaction #52035
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCN(CCF)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53936
trans-N-(4-{5-[Ethyl-(2-fluoro-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
Выход 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
FCCC#Cc1cccc(Br)c1
Reaction #58845
1-Bromo-3-(4-fluoro-but-1-ynyl)benzene
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
FCCCCCc1cccc(Br)c1
Reaction #58859
1-bromo-3-(5-fluoropentyl)benzene
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)CC(c2ccccc2N2CCN(C[C@@H]3C[C@H]3CF)CC2)CC(C)(C)C1
Reaction #60510
trans-1-(2-fluoromethylcyclopropylmethyl)-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
Выход 28.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc2c(cc1O)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@H](F)CC[C@@H]12
Reaction #60576
17α-fluoro-3-hydroxy-2-methoxy-estra-1,3,5(10)-triene
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)N1CCc2c(c(-c3ccc(C(F)(F)F)cc3)nn2CC(F)CN2CCN(c3ccccc3C#N)CC2)C1
Reaction #61864
title compound
Выход 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(C)OC
Reaction #66651
5-[2-Isopropyl-4-methoxy-5-(1-methoxy-ethyl)-phenoxy]-pyrimidine-2,4-diamine
Выход 4.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(Cl)cc(Oc2cnc(N)nc2N)c1C(C)(C)F
Reaction #66655
5-[5-Chloro-2-(1-fluoro-1-methyl-ethyl)-methoxy-phenoxy]-pyrimidine-2,4-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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