1,1-dichloroethane

CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC1CCC(n2cc(C)c(=O)[nH]c2=O)O1
Reaction #1652
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1CC(S(=O)(=O)c2ccccc2)C1C(=O)OC
Reaction #6069
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Br
Reaction #6124
expected product
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)Nc1ccc(Sc2nc(Nc3cc(C)n[nH]3)c3ccc(O)cc3n2)cc1
Reaction #7705
[2-(4-acetamidophenylsulfanyl)-7-hydroxy-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)Nc1ccc(Sc2nc(Nc3cc(C)n[nH]3)cc(-c3ccc(O)cc3)n2)cc1
Reaction #7711
[2-(4-acetamido-phenyl-sulfanyl)-6-(4-hydroxyphenyl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(Cl)c1ccc2ncsc2c1
Reaction #8940
6-Chlorosulfonylbenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2=O
Reaction #9340
15-8
Выход 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(Cl)ccc2c1C(=O)CC2
Reaction #9378
6-chloro-7-methyl-1-indanone
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCc2ccc(Cl)c(Cl)c21
Reaction #9379
6,7-dichloro-1-indanone
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(CC(=O)c1ccc(Br)cc1)C(=O)O
Reaction #9615
4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc2nc(Nc3ccc(-c4ccc(C(=O)CC(C)(C)C(=O)O)cc4)cc3)oc2c1
Reaction #9698
2,2-dimethyl 4-{4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}4-oxobutanoic acid
Выход 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc2oc(Nc3ccc(-c4ccc(C(=O)CC(C)(C)C(=O)O)cc4)cc3)nc12
Reaction #9699
2,2-dimethyl-4-{4′-[(4-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}4-oxobutanoic acid
Выход 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)C1CCCC1C(=O)c1ccc(-c2ccc(Nc3nc4cc(F)ccc4o3)cc2)cc1
Reaction #9700
2-({4′-[(5-fluoro-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Выход 31.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(C)cc4o3)c(F)c2)cc1
Reaction #9701
methyl (1R,2R)-2-({3′-fluoro-4′-[(6-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)-cyclopentanecarboxylate
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(Cl)c1ccc2ncsc2c1
Reaction #11347
6-Chlorosulfonylbenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NS(=O)(=O)Cc1cc(Cl)ccc1O
Reaction #11765
title compound
Выход 86.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)[C@@H]1C[C@H](OC(=N)C(Cl)(Cl)Cl)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40596
21
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41036
title compound
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccsc1-c1cn(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)c(=O)[nH]c1=O.Cl
Reaction #41040
title compound
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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