Impliqué dans 30 réactions

1265839

CC1(O)CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #176462

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CC(C)(C)[Si](C)(C)OC1CCCC(n2nc(-c3c(-c4ccccc4)nn4ccccc34)ccc2=O)C1

Reaction #185521

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

O=c1ccc(-c2c(-c3ccccc3)nn3ccccc23)nn1C1CCCCC1O

Reaction #267395

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

CC1(C)Oc2ccc(C#N)cc2C(n2nc(-c3c(-c4ccccc4)nn4ccccc34)ccc2=O)C1O

Reaction #288728

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

Clc1ccc(-c2c(-c3ccccc3)nn3ccccc23)nn1

Reaction #300747

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)

$COC(=O)/C=C1\CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O$

Reaction #364121

(E)-3-[2-(2-methoxycarbonylmethylenecyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 46.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03

CC(C)(C)[Si](C)(C)OC1CCCC(n2nc(-c3c(-c4ccccc4)nn4ccccc34)ccc2=O)C1

Reaction #364122

3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Rendement 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03

C[C@@]1(O)CCCC[C@H]1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #364123

3-[2-{(1R*,2R*)-2-hydroxy-2-methylcyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Rendement 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03

CC(C)(C)[Si](C)(C)OC1CCCC(n2nc(-c3c(-c4ccccc4)nn4ccccc34)ccc2=O)C1

Reaction #379746

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)

COC(=O)CCn1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #553180

3-[2-(2-methoxycarbonylethyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10

CCOC(=O)CCCn1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #553200

3-[2-(3-ethoxycarbonylpropyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 74.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10

Clc1ccc(-c2c(-c3ccccc3)nn3ccccc23)nn1

Reaction #553210

3-(3-chloropyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10

CCOC(=O)CCCn1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #791159

3-[2-(3-ethoxycarbonylpropyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 74.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_01

Clc1ccc(-c2c(-c3ccccc3)nn3ccccc23)nn1

Reaction #791170

3-(3-chloropyridazin-6-yl)-2-phenylpyrazolo[1,5-a]pyridine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_01

COC(=O)C=C1CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #921722

DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D

O=c1ccc(-c2c(-c3ccccc3)nn3ccccc23)nn1[C@@H]1CCCC[C@@H]1O

Reaction #1052527

cis-3-[2-(2-hydroxycyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 3.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06

$COC(=O)/C=C1\CCCCC1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O$

Reaction #1052531

(E)-3-[2-(2-methoxycarbonylmethylenecyclohexyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine

Rendement 46.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06

CC(C)(C)[Si](C)(C)OC1CCCC(n2nc(-c3c(-c4ccccc4)nn4ccccc34)ccc2=O)C1

Reaction #1052532

3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1, 5-a]-pyridine

Rendement 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06

C[C@@]1(O)CCCC[C@H]1n1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #1052533

3-[2-{(1R*,2R*)-2-hydroxy-2-methylcyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Rendement 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06

CCOC(=O)CCCn1nc(-c2c(-c3ccccc3)nn3ccccc23)ccc1=O

Reaction #1297892

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)