propargyltrifluoroacetamide

O=C(NCC#Cc1cn([C@H]2CC[C@@H](CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #4985
alkynylamino nucleoside
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1nc(=O)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)cc1C#CCNC(=O)C(F)(F)F
Reaction #71512
5-[3-(trifluoroacetamido)propynyl]cytidine
수율 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCC#Cc1cn(C2OC(CO)C(O)C2O)c(=O)[nH]c1=O)C(F)(F)F
Reaction #178653
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc(=O)n(C2OC(CO)C(O)C2O)cc1C#CCNC(=O)C(F)(F)F
Reaction #194406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCC1OC(O)C(O)C1O
Reaction #199279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #205908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc(=O)n(COCCO)cc1C#CCNC(=O)C(F)(F)F
Reaction #235610
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ncnc2[nH]nc(C#CCNC(=O)C(F)(F)F)c12
Reaction #271431
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCC#Cc1cn(C2CC(O)C(CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #289642
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1nc(=O)n(C2CC(O)C(CO)O2)cc1C#CCNC(=O)C(F)(F)F
Reaction #373974
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCC(O)(C#Cc1cccc(C#CCNC(=O)C(F)(F)F)c1)CCC
Reaction #428803
2,2,2-trifluoro-N-(3-(3-(3-hydroxy-3-propylhex-1-ynyl)phenyl)prop-2-ynyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCC(O)(C#Cc1cccc(C#CCNC(=O)C(F)(F)F)c1)CCC
Reaction #541584
2,2,2-trifluoro-N-(3-(3-(3-hydroxy-3-propylhex-1-ynyl)phenyl)prop-2-ynyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCNC(=O)C(F)(F)F
Reaction #584163
trifluoro-N-propylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
O=C(NCC#Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #587483
crystals
수율 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
Nc1nc(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1C#CCNC(=O)C(F)(F)F
Reaction #587488
expected product ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C=CCO[C@H]1C[C@H](n2cc(C#CCNC(=O)C(F)(F)F)c(=O)[nH]c2=O)O[C@@H]1CO
Reaction #587496
crystals
수율 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCCC(O)(C#Cc1cccc(C#CCNC(=O)C(F)(F)F)c1)CCC
Reaction #604339
2,2,2-trifluoro-N-(3-(3-(3-hydroxy-3-propylhex-1-ynyl)phenyl)prop-2-ynyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
O=C(NCC#Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O)C(F)(F)F
Reaction #743851
crystals
수율 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
Nc1nc(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1C#CCNC(=O)C(F)(F)F
Reaction #743856
expected product ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
C=CCO[C@H]1C[C@H](n2cc(C#CCNC(=O)C(F)(F)F)c(=O)[nH]c2=O)O[C@@H]1CO
Reaction #743862
crystals
수율 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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