4-chloro-2,6-diaminopyrimidine

Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
المردود 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)[n+]1c(-c2ccco2)c(NC2CCCCC2)n2c(N)cc(Cl)nc21.[Cl-]
Reaction #7616
1-acetyl-5-amino-7-chloro-3-cyclohexylamino-2-furan-2-yl-imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(-c2ccccn2)c(NC2CCCCC2)n2c(N)cc(Cl)nc21.[Cl-]
Reaction #7622
1-acetyl-5-amino-7-chloro-3-cyclohexylamino-2-pyridin-2-yl-imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(C)c(NC2CCCCC2)n2c(N)cc(Cl)nc21.[Cl-]
Reaction #7627
1-acetyl-5-amino-7-chloro-3-cyclohexylamino-2-methyl-imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(-c2cccs2)c(NC2CCCCC2)n2c(N)cc(Cl)nc21.[Cl-]
Reaction #7628
1-acetyl-5-amino-7-chloro-3-cyclohexylamino-2-thiophene-2-yl-imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)CNc1c(-c2ccco2)[n+](C(C)=O)c2nc(Cl)cc(N)n12.[Cl-]
Reaction #7629
1-acetyl-5-amino-7-chloro-2-furan-2-yl-3-(methoxycarbonylmethylamino)imidazo[1,2-a]pyrimidin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #54683
2,4-diamino-6-chloro-pyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #54684
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #54716
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #55501
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #55502
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75095
2,4-diamino-6-chloro-pyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75096
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75108
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75109
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75297
2,4-diamino-6-chloro-pyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75298
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #207292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(N)c1cc(N)nc(N)n1
Reaction #214371
2,4-diamino-6-(1-methylhydrazino)pyrimidine
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #214858
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
الصفحة 1التالي