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1269917

O=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162121
29b
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162122
(3S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162159
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162189
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162191
62a
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@]1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162196
63a
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCC(=O)C4)n3)c3cc(Cl)cnc32)cc1
Reaction #162199
64a
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614146
29b
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614147
(3S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)-1-methylcyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614185
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614224
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614231
62a
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@]1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #614235
63a
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCC(=O)C4)n3)c3cc(Cl)cnc32)cc1
Reaction #614238
64a
DOI: 10.6084/m9.figshare.5104873.v1