参与 20 个反应

17821

ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #8601
2-(4chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #8602
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #749417
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #811166
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #983964
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_07
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #983965
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_07
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1150046
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1150047
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1150065
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1150066
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1460591
2-(4-chloro-2pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1460592
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_01
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1883726
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1883727
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1883747
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1883748
5-chloro-2-(4-fluorophenyl)-pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #1884237
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #1884238
5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
ON=C(Cc1cc(Cl)ccn1)c1ccc(F)cc1
Reaction #2302115
2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_09
Fc1ccc(-c2cc3cc(Cl)ccn3n2)cc1
Reaction #2302116
5-chloro-2-(4 fluorophenyl)pyrazolo[1,5-α]pyridine
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_09