1-bromo-3-fluorobenzene

CN(C)C(=O)c1cc(C2CCCN2c2cccc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #503
Ausbeute 41.1%750 AstraZeneca ELN dataset
COC(=O)c1cc(C2CCCN2c2cccc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #511
Ausbeute 78.6%750 AstraZeneca ELN dataset
COC(=O)c1cc(C2CCCN2c2cccc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #569
Ausbeute 70.8%750 AstraZeneca ELN dataset
O=Cc1c(F)cccc1Br
Reaction #43678
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(C(=O)c1cccc(F)c1)c1cccc(F)c1
Reaction #46988
product 20
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc([C@H]2CCCN2c2cccc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #69470
methyl 8-[(2R)-(1-(3-fluorophenyl)pyrrolidin-2-yl)]-2-morpholino-4-oxo-4H-chromene-6-carboxylate
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)C(=O)c1cc(C2CCCN2c2cccc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #69483
8-(1-(3-fluorophenyl)pyrrolidin-2-yl)-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide
Ausbeute 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(C2CCCN2c2cccc(F)c2)c2oc(N3CCO[C@H](C)C3)cc(=O)c2c1
Reaction #69503
methyl 8-(1-(3-fluorophenyl)pyrrolidin-2-yl)-2-((R)-2-methylmorpholino)-4-oxo-4H-chromene-6-carboxylate
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCC1CCC(O)(c2cccc(F)c2)CC1
Reaction #189361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1c(F)cccc1Br
Reaction #192136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)OC(=O)Nc2ccc(-c3cccc(F)c3)cc21
Reaction #205144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccccc1C(=O)c1cccc(F)c1
Reaction #220442
2-Amino-3′-fluorobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCC(=O)c1ccc(Br)cc1F
Reaction #234086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1ccc(CC(=O)c2cccc(F)c2)cc1
Reaction #234318
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)Cc1c(C(=O)c2cccc(F)c2)[nH]c2cc(Cl)ccc12
Reaction #239005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1-c1cccc(-n2cnc(C(=O)c3cccc(F)c3)c2)c1
Reaction #248589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=Cc1c(F)cccc1Br
Reaction #250559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(Oc2cccc(F)c2)c(C(O)=S)c1
Reaction #253912
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=Cc1c(F)cccc1Br
Reaction #274295
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1c(F)cccc1-c1cccc(-n2cnc(C(=O)c3cccc(F)c3)c2)c1
Reaction #283092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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