Recherche de Sous-structure

1422577

CCCCn1c(=O)c2[nH]c([N+](=O)[O-])nc2n(CCCC)c1=O
Reaction #3724
1,3-Di-n-butyl-8-nitro Xanthine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2[nH]c([N+](=O)[O-])nc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3725
product
Rendement 56.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1c(=O)c2[nH]c(N)nc2n(CCCC)c1=O.Cl
Reaction #3726
1,3-Di-n-butyl-8-amino Xanthine Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc2c([nH]1)c(=O)n(C1CC1)c(=O)n2C1CC1
Reaction #3727
1,3-Di-cyclopropyl-8-amino Xanthine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1c(=O)c2[nH]c(Cl)nc2n(CCCC)c1=O
Reaction #3729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1c(=O)c2[nH]c(Br)nc2n(CCCC)c1=O
Reaction #3730
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2[nH]c(Cl)nc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3731
1,3-Di-cyclopropylmethyl-8-chloro Xanthine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2[nH]c(Cl)nc2n(C2CCCCC2)c(=O)n1C1CCCCC1
Reaction #3732
1,3-Di-cyclohexyl-8-chloro xanthine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2[nH]c(Br)nc2n(CC2CCCCC2)c(=O)n1CC1CCCCC1
Reaction #3738
title product
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1ccnc1N
Reaction #71339
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1ccnc1[N+](=O)[O-]
Reaction #71340
title compound
Rendement 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)Cc1c[nH]c([N+](=O)[O-])n1
Reaction #71341
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2c[nH]c(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)n2)CC1
Reaction #71359
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2c[nH]c(NC(=O)c3ccc(-c4csc5ccccc45)c4nccnc34)n2)CC1
Reaction #71368
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cscc1-c1ccc(C(=O)Nc2nc(CN3CCN(C)CC3)c[nH]2)c2nccnc12
Reaction #71375
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C)c1-c1ccc(C(=O)Nc2nc(CN3CCN(C)CC3)c[nH]2)c2nccnc12
Reaction #71380
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3nc(CN4CCCC4)c[nH]3)c3nccnc23)c1F
Reaction #71399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3nc(CN4CCCC4)c[nH]3)c3nccnc23)c1
Reaction #71404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3nc(CN(C)C)c[nH]3)c3nccnc23)c1F
Reaction #71441
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3nc(CN4CCOCC4)c[nH]3)c3nccnc23)c1F
Reaction #71446
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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