Adenine

CCOP(=O)(COCOCn1cnc2c(N)ncnc21)OCC
Reaction #1649
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1CCC1n1cnc2c(N)ncnc21
Reaction #6049
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1F
Reaction #65347
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1cccc2nc(C(C)n3cnc4c(N)ncnc43)c(Br)c(=O)n12
Reaction #86498
desired product
Ausbeute 10.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ncnc2c1ncn2CCO
Reaction #220296
9-(2-hydroxyethyl)adenine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C[C@@H](O)Cn1cnc2c(N)ncnc21
Reaction #220298
(R)-9-[2-(hydroxy)propyl]adenine
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1cc2nc(Cn3cnc4c(N)ncnc43)n(-c3ccccc3Cl)c(=O)c2cc1OC
Reaction #329101
beige solid
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1ncnc2c1ncn2Cc1nc2ccc(Cl)cc2c(=O)n1-c1ccccc1Cl
Reaction #329102
yellow solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1ncnc2c1ncn2Cc1nc2cccc(F)c2c(=O)n1-c1ccccc1Cl
Reaction #329103
off-white solid
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cccc2nc(Cn3cnc4c(N)ncnc43)n(-c3ccccc3Cl)c(=O)c12
Reaction #329104
pale yellow solid
Ausbeute 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1ncnc2c1ncn2Cc1nc2c(Cl)cccc2c(=O)n1-c1ccccc1Cl
Reaction #329105
pale yellow solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1ncnc2c1ncn2Cc1nc2cccc(Cl)c2c(=O)n1-c1ccccc1F
Reaction #329108
tan solid
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cccc2nc(Cn3cnc4c(N)ncnc43)n(-c3ccccc3C(C)C)c(=O)c12
Reaction #329121
2-(6-Aminopurin-9-ylmethyl)-3-(2-isopropylphenyl)-5-methyl-3H-quinazolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1ccccc1-n1c(Cn2cnc3c(N)ncnc32)nc2cccc(C)c2c1=O
Reaction #329122
2-(6-Aminopurin-9-ylmethyl)-5-methyl-3-o-tolyl-3H-quinazolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccccc1-n1c(Cn2cnc3c(N)ncnc32)nc2cccc(Cl)c2c1=O
Reaction #329124
brown solid
Ausbeute 38.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC#Cc1c[nH]c(=O)[nH]c1=O
Reaction #340111
5-propynyluracil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Nc1ncnc2c1ncn2C=CCCN1C(=O)c2ccccc2C1=O
Reaction #347449
expected product
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
Nc1ncnc2c1ncn2CCCCOCP(=O)(O)O
Reaction #353424
material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Nc1ncnc2c1ncn2CCO
Reaction #423239
9-(2-hydroxyethyl)adenine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOP(=O)(COC(OC)n1cnc2c(N)ncnc21)OCC
Reaction #443913
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
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