2-fluoroethanamine

FCCNC1CCC(Nc2cccc3cnccc23)CC1
Reaction #197152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)Cc1c(Cl)ccc2ccc(CNCCF)cc12
Reaction #198502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(c1ccc(Br)cc1)N1CCC(CCNCCF)(c2ccc(F)cc2)OC1=O
Reaction #209273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC(Cc1ccc(OC(F)(F)F)cc1)C(=O)NCCF)c1ccc(OCCC(F)(F)F)cc1
Reaction #283612
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FCCNC1CCC(Nc2ccc3[nH]ncc3c2)CC1
Reaction #285265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FCCNc1nc2ccc(Br)cc2s1
Reaction #286853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1c(=O)sc2cc(N3CC(C(=O)NCCF)OC3=O)ccc21
Reaction #301387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CNC(=O)c1sc(C2=NOC(c3cc(Cl)c(F)c(Cl)c3)(C(F)(F)F)C2)c2c1CCC2)NCCF
Reaction #328089
desired product
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(NCCF)NC1Cc2cccc(F)c2C1
Reaction #385611
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1COCCN1c1nc(-c2ccc(NC(=O)NCCF)cc2)nc2c1CCN(c1ncccn1)C2
Reaction #394926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CNC(=O)c1ccc2nonc2c1)NCCF
Reaction #402836
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN1CCN(c2ccccc2CNC(=O)c2ccc(F)c(NC(=O)c3cnc4cc(-c5ccc(C(=O)NCCF)c(F)c5)ccn34)c2)CC1
Reaction #422483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(CNC(=O)c1sc(C2=NOC(c3cc(Cl)c(F)c(Cl)c3)(C(F)(F)F)C2)c2c1CCC2)NCCF
Reaction #424199
desired product
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(NCCF)Oc1ccccc1
Reaction #475062
title compound
Ausbeute 86.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCn1c(Nc2nc3ccc(Cl)cc3s2)nc2cc(C(=O)NCCF)ccc21
Reaction #498104
2-(6-Chloro-benzothiazol-2-ylamino)-1-ethyl-1H-benzoimidazole-5-carboxylic acid (2-fluoro-ethyl)-amide
Ausbeute 44.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CN(C)C(=O)CCCC#Cc1cccc(C(=O)NCCF)c1
Reaction #730229
3-(5-dimethylcarbamoyl-pent-1-ynyl)-N-(2-fluoro-ethyl)benzamide
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=S1(=O)NC2(CCCC2)C(CNCCF)=C1c1ccc(Cl)cc1
Reaction #769361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(NCCF)c1cn(CC(=O)Nc2sc3c(c2C(N)=O)CCCC3)nc1C(F)(F)F
Reaction #775021
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Nc1c(C(=O)NCC(O)(CNCCF)C(F)(F)F)cnn1-c1ccc(F)cc1
Reaction #783205
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc2nccc(Oc3ccc(NC(=O)NCCF)c(F)c3)c2cc1OC
Reaction #784190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
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