6-chloropurine

CC(=O)c1cc(Nc2ncnc3nc[nH]c23)cc(C(C)=O)c1
Reaction #3491
6-[(3,5-diacetylphenyl)amino]purine
المردود 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON(C)C(C)CNc1ncnc2nc[nH]c12
Reaction #5370
white crystals
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@H]1[C@@H](NC(=O)Cc2cccc3c2Cc2ccccc2-3)[C@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@@H]1n1cnc2c(Cl)ncnc21
Reaction #58428
7
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1nc(NC2CC2)c2nc[nH]c2n1
Reaction #65352
cream solid
المردود 153.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
c1ccc(-c2ccc3nnc(CNc4ncnc5nc[nH]c45)n3n2)cc1
Reaction #68492
N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7H-purin-6-amine
المردود 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc2c(c1)CC(Nc1ncnc3nc[nH]c13)C2
Reaction #76724
title compound
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Brc1cccc(Nc2ncnc3nc[nH]c23)c1
Reaction #79128
N6-(3-bromophenyl)adenine
المردود 102.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(=O)c1cc(Nc2ncnc3nc[nH]c23)cc(C(C)=O)c1
Reaction #81894
6-[(3,5-diacetylphenyl)amino]purine
المردود 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1csc2nc([C@H](C)Nc3ncnc4[nH]cnc34)c(-c3cccc(F)c3)c(=O)n12
Reaction #86530
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(n4cnc5c(Cl)ncnc54)=C(C=O)C[C@@H]32)C1
Reaction #87331
21a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N[C@@]1(C(=O)O)CN(c2ncnc3nc[nH]c23)C[C@@H]1CCCB(O)O
Reaction #89647
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(7H-purin-6-yl)pyrrolidine-3-carboxylic acid
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccc2c(OC[C@H]3CCCN3c3ncnc4[nH]cnc34)cccc2c1
Reaction #168570
colourless crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
F[C@H]1C[C@H](COc2ccccc2Cl)N(c2ncnc3[nH]cnc23)C1
Reaction #168577
6-[(2R,4S)-2-(2-chlorophenoxymethyl)-4-fluoropyrrolidin-1-yl]-9H-purine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1cccc(/C=C/[C@H]2CCCN2c2ncnc3[nH]cnc23)c1
Reaction #168581
6-[(R)-2-((E)-2-(3-chlorophenyl)vinyl)pyrrolidin-1-yl]-9H-purine
المردود 16.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Fc1ccc(OCc2ccccc2)c(-c2nc3c(Cl)cccc3cc2CNc2ncnc3[nH]cnc23)c1
Reaction #186015
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCCOCn1cnc2c(Cl)ncnc21)c1ccccc1
Reaction #187646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc(CNc2ncnc3c2ncn3C2CCCO2)cc1
Reaction #187739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cc(F)cc(-c2nc3c(Cl)cccc3cc2CNc2ncnc3[nH]cnc23)c1
Reaction #196483
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1cccc(OCCCCCn2cnc3c(Cl)ncnc32)c1
Reaction #201616
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)[Si](C)(C)OC(O)[C@@H](O)[C@](O)(O[Si](C)(C)C(C)(C)C)C(F)(F)C(=O)n1cnc2c(Cl)ncnc21
Reaction #215750
1-(6-chloro-9H-purin-9-yl)-3,5-bis(t-butyldimethylsiloxy)-2-desoxy-2,2-difluororibose
المردود 34.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
الصفحة 1التالي