iron

Nc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #1582
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCc1cc2c(cc1Br)CCCCC2(C)C
Reaction #1733
2-bromo-3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Cl)c(F)cn1
Reaction #1954
title compound
Выход 142.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1nc2ccc(N)cc2c(O)c1C(=O)OCC
Reaction #3229
title compound
Выход 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(N)cnc1Cl
Reaction #3415
solid
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)N1CCc2cc(Br)cc(N)c21
Reaction #5023
compound
Выход 32.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc(F)c(N)cc1O
Reaction #7577
2-fluoro-5-hydroxy-4-methylaniline
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(F)c(N)cc1OCc1ccccc1
Reaction #7592
5-benzyloxy-2-fluoro-4-methylaniline
Выход 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)Nc1ccc(Sc2nc(Nc3cc(C)n[nH]3)c3ccc(N)cc3n2)cc1
Reaction #7707
[2-(4-acetamido-phenylsulfanyl)-7-aminoquinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCCCCCN
Reaction #8662
hexamethylenediamine
Выход 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCCCCCN
Reaction #8663
hexamethylenediamine
Выход 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(-c2nc3ccccc3[nH]2)cc1
Reaction #9062
methyl 4-(benzimidazol-2-yl)-benzoate
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(CCc1ccccc1)CC(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9622
ethyl 4-(4′-amino-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1(CC(=O)c2ccc(-c3ccc(N)cc3)cc2)CCOCC1
Reaction #9633
methyl 4-[2-(4′-amino-1,1′-biphenyl-4-yl)-2-oxoethyl]tetrahydro-2H-pyran-4-carboxylate
Выход 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(OC)c2)cc1
Reaction #9653
methyl 4-(4′-amino-3′-methoxy-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Reaction #9658
solid
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1Nc2ccc(Cl)c(Cl)c2N2CCN(C(=O)OCc3ccccc3)CC12
Reaction #11906
desired product
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCSc1c(Cl)cc2c([nH]c3cnccc32)c1N
Reaction #40480
6-chloro-7-ethylsulfanyl-9H-β-carbolin-8-ylamine
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCSc1c(Cl)cc2c([nH]c3cnccc32)c1N
Reaction #40483
6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine
Выход 107.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Oc2cccnc2)c(Cl)c1Oc1cccnc1
Reaction #41533
3-chloro-2,4-bis(pyridin-3-yloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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