Participa en 37 reacciones

5857

Cn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
Reaction #2091
7-Benzyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #2092
7-Benzyl-1-ethoxymethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O)OCC
Reaction #2112
Diethyl [4-(7-benzyl-3-methylxanthin-1-yl)butyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O)OCC
Reaction #2131
Diethyl [7-benzyl-3-(3-methylxanthin-1-yl)propyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O)OCC
Reaction #2132
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
Reaction #231919
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1c(=O)n(COc2ccc(Cl)cc2)c(=O)c2c1ncn2Cc1ccccc1
Reaction #399469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
Reaction #411032
7-Benzyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC(C)COCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #411051
7-Benzyl-1-isobutoxymethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COCCOCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #411053
7-Benzyl-1-(2-methoxyethoxymethyl)-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cn1c(=O)n(CCOc2ccccc2)c(=O)c2c1ncn2Cc1ccccc1
Reaction #411055
7-Benzyl-3-methyl-1-(2-phenoxyethyl)xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cn1c(=O)n(COc2ccc(Cl)cc2)c(=O)c2c1ncn2Cc1ccccc1
Reaction #411056
7-Benzyl-1-(4-chlorophenoxymethyl)-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC(=O)OC(C)CCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #781819
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)COCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #889116
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(=O)OC(C)CCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #898454
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cn1c(=O)n(COC(=O)C(C)(C)C)c(=O)c2c1ncn2Cc1ccccc1
Reaction #920562
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(=O)CCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #1027792
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
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Reaction #1134277
2.7
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
Cn1c(=O)n(CCOc2ccccc2)c(=O)c2c1ncn2Cc1ccccc1
Reaction #1229583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CCOP(=O)(CCCCCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O)OCC
Reaction #1303311
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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