Участвует в 28 реакциях

O=Cc1nn(C2CCCCO2)c2ccc(I)cc12

O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #156103
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1nn(C2CCCCO2)c2ccc(-c3cncc(C(=O)NCC4CC4)c3)cc12
Reaction #156109
N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #177190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #964297
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
—
Reaction #964318
solid
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #976311
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
O=Cc1nn(C2CCCCO2)c2ccc(-c3cncc(C(=O)NCC4CC4)c3)cc12
Reaction #976317
N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1135846
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
O=Cc1nn(C2CCCCO2)c2ccc(-c3cncc(C(=O)NCC4CC4)c3)cc12
Reaction #1135852
N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1270227
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
—
Reaction #1270248
solid
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1274515
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
—
Reaction #1274536
solid
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1585009
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carb aldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
—
Reaction #1585030
solid
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1594292
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
CN(C)C(=O)Nc1cncc(-c2ccc3c(c2)c(C=O)nn3C2CCCCO2)c1
Reaction #1594298
3-(5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)pyridin-3-yl)-1,1-dimethylurea
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=Cc1nn(C2CCCCO2)c2ccc(-c3cccnc3)cc12
Reaction #1594305
5-(pyridin-3-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
O=Cc1nn(C2CCCCO2)c2ccc(I)cc12
Reaction #1616368
5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
O=Cc1nn(C2CCCCO2)c2ccc(-c3cncc(C(=O)NCC4CC4)c3)cc12
Reaction #1616374
N-(cyclopropylmethyl)-5-(3-formyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)nicotinamide
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
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