2,6-diamino-4-hydroxypyrimidine

Nc1nc(O)c2cc[nH]c2n1
Reaction #50298
2-amino-4 -hydroxy-7H-pyrrolo[2,3-d]pyrimidine
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)c1ccc(CCc2c[nH]c3nc(N)[nH]c(=O)c23)cc1
Reaction #65045
4-(2-[2-amino-4-oxo-3,7-dihydropyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acid methyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
—
Reaction #65050
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Nc1nc(N)c(N=O)c(O)n1
Reaction #268011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(CCc2c[nH]c3nc(N)[nH]c(=O)c23)cc1
Reaction #350887
4-(2-[2-amino-4-oxo-3,7-dihydropyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acid methyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Nc1nc2[nH]ccc2c(=O)[nH]1
Reaction #505013
title compound
Yield 52.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)c1ccc(CCc2c[nH]c3nc(N)[nH]c(=O)c23)cc1
Reaction #530197
4-(2-[2-amino-4-oxo-3,7-dihydropyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acid methyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
—
Reaction #530201
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
COC(=O)c1ccc(-c2cc3c(O)nc(N)nc3[nH]2)cc1
Reaction #677804
Methyl 4-(2-amino-4-hydroxy-7H-pyrrolo[2,3-d]pyrimidin-6-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
N#Cc1ccc(-c2cc3c(O)nc(N)nc3[nH]2)cc1
Reaction #677805
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOc1cc(N)nc(N)n1
Reaction #773932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)c1c[nH]c2nc(N)[nH]c(=O)c12
Reaction #809429
2-amino-5-isopropyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COC(=O)c1ccc(CCc2c[nH]c3nc(N)[nH]c(=O)c23)cc1
Reaction #1064131
4-(2-[2-amino-4-oxo-3,7-dihydropyrrolo[2,3 -d]pyrimidin-5-yl]ethyl)benzoic acid methyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
Cc1ccc(S(=O)(=O)O)cc1
Reaction #1064136
p-toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
COC(=O)C1=C(COCCn2c(C)nc(C)c2C)Nc2[nH]c(N)nc(=O)c2C1c1ccccc1Cl
Reaction #1068703
title compound
Yield 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_02
Nc1nc(N)c(N=O)c(O)n1
Reaction #1265404
title compound
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
COC(=O)c1ccc(C(O)Cn2ccc3nc(N)nc(O)c32)cc1
Reaction #1285120
product
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_01
c1ncc2nc3cncnc3nc2n1
Reaction #1446639
pyrimido[5,4-g]pteridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
c1ncc2nc3cncnc3nc2n1
Reaction #1446640
pyrimido-[5,4-g]pteridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
COC(=O)c1ccc(CCc2c[nH]c3nc(N)[nH]c(=O)c23)cc1
Reaction #1463925
4-(2-[2-amino-4-oxo-3,7-dihydropyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acid methyl ester
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
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