Impliqué dans 8 réactions

4903853

Cc1ccc(N)c(Cl)c1Oc1ccc2nc(NC(=O)C3CC3)cn2n1

Reaction #198329

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

$CC1=C/C(=N\c2c(N)n3n(c2=O)CCC3)C(N)=C(Cl)C1=O$

Reaction #816363

3-amino-2-{[(1E)-2-amino-3-chloro-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene]amino}-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09

CC1=CC(=Nc2c(N)n3n(c2=O)CCCC3)C(N)=C(Cl)C1=O

Reaction #816370

3-amino-2-[(2-amino-3-chloro-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)amino]-5,6,7,8-tetra-hydro-1H-pyrazolo[1,2-a]pyridazin-1-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09

CC1=CC(=Nc2c(N)n3n(c2=O)CCN(C)CC3)C(N)=C(Cl)C1=O

Reaction #816371

9-amino-8-[(2-amino-3-chloro-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)amino]-3-methyl-2,3,4,5-tetrahydro-1H,7H-pyrazolo[1,2-a][1,2,5]triazepin-7-one

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09

$CC1=C/C(=N\c2c(NCC[N+](C)(C)C)nn3ccccc23)C(N)=C(Cl)C1=O.[Cl-]$

Reaction #1451037

2-[(3-{[(1E)-2-amino-3-chloro-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene]amino}pyrazolo[1,5-a]pyridin-2-yl)amino]-N,N,N-trimethylethanaminium chloride

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02

Cc1ccc(N)c(Cl)c1Oc1ccc2nc(NC(=O)C3CC3)cn2n1

Reaction #1751155

Rendement 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10

Cc1ccc(N)c(Cl)c1Oc1ccc2nc(NC(=O)C3CC3)cn2n1

Reaction #1755345

Rendement 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10

Cc1ccc(N)c(Cl)c1Oc1ccc2nc(NC(=O)C3CC3)cn2n1

Reaction #2478652

Rendement 64.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09