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8623

CCOP(=O)(COC(CONc1ncnc(Cl)c1NC=O)COC(C)=O)OCC
Reaction #6344
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COC(CONc1nc(NC=O)nc(Cl)c1NC=O)COC(C)=O)OCC
Reaction #6345
title compound
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1nc(Cl)c(NC=O)c(NOCc2ccccc2)n1
Reaction #6349
title compound
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1c(Cl)cccc1Cl)Nc1c(Cl)ncnc1Cl
Reaction #88464
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Cl)c1Cc1nc2c(Cl)ncnc2o1
Reaction #88465
solid
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ncnc2sc(Cc3c(Cl)cccc3Cl)nc12
Reaction #88466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc(SC)nc2sc(Cc3c(Cl)cccc3Cl)nc12
Reaction #88467
2-(2,6-dichloro-benzyl)-7-ethoxy-5-methylsulfanyl-thiazolo[5,4-d]pyrimidine
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(CONc2nc(NC=O)nc(Cl)c2NC=O)O1
Reaction #221484
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccccc1)c1c(N)ncnc1Cl
Reaction #265588
DOI: 10.1039/C8SC04228D
CCOP(=O)(COCCCONc1ncnc(Cl)c1NC=O)OCC
Reaction #266985
DOI: 10.1039/C8SC04228D
CCc1nn(C2CCCC2)c2cc(C(=O)Nc3c(Cl)ncnc3Cl)ccc12
Reaction #281450
DOI: 10.1039/C8SC04228D
CCOP(=O)(COCCCONc1nc(NC=O)nc(Cl)c1NC=O)OCC
Reaction #284057
DOI: 10.1039/C8SC04228D
Nc1nc(Cl)c(NC=O)c(NC2C=CC(CO)C2)n1
Reaction #290837
DOI: 10.1039/C8SC04228D
Nc1nc(Cl)c(NC=O)c(NC2CC=C(CO)C2)n1
Reaction #292207
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccccc1)c1c(Cl)ncnc1Cl
Reaction #296318
DOI: 10.1039/C8SC04228D
CCOP(=O)(COCCCONc1nc(NC=O)nc(Cl)c1NC=O)OCC
Reaction #432238
4-chloro-6-[3-(diethoxyphosphorylmethoxy)propoxyamino]-2,5-diformamidopyrimidine
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(COCCCONc1ncnc(Cl)c1NC=O)OCC
Reaction #432240
4-chloro-6-[3-(diethoxyphosphorylmethoxy)propoxyamino]-5-formamidopyrimidine
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)c(NC=O)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #456686
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCONc1nc(NC=O)nc(Cl)c1NC=O)OCC
Reaction #461057
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCONc1nc(NC=O)nc(Cl)c1NC=O)OCC
Reaction #461060
title compound
Ausbeute 83.7%DOI: 10.6084/m9.figshare.5104873.v1
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