4-chloro-7H-pyrrolo[2,3-d]pyrimidine

Clc1ncnc2[nH]cc(I)c12
Reaction #10256
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1ncnc2[nH]cc(I)c12
Reaction #169435
4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCCC12CCCN(c1ncnc3[nH]ccc13)C2
Reaction #184629
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNCC1(c2ccc(Cl)cc2)CCN(c2ncnc3[nH]ccc23)CC1
Reaction #185478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ncnc2[nH]cc(I)c12
Reaction #195713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(n2ccc3c(Cl)ncnc32)CC1
Reaction #209790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)n2ccc3c(Cl)ncnc32)cc1
Reaction #221645
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ncnc2[nH]ccc12
Reaction #223600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ncccc1-c1ncnc2[nH]ccc12
Reaction #226127
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(S(=O)(=O)n2ccc3c(Cl)ncnc32)cc1
Reaction #230850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Ic1ncnc2[nH]ccc12
Reaction #240376
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ncc2cc[nH]c2n1
Reaction #242865
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ncc(F)cc1CN(C(=O)OC(C)(C)C)c1ccc(C(O)c2c[nH]c3ncnc(Cl)c23)cn1
Reaction #243426
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1c[nH]c2ncnc(Cl)c12
Reaction #251309
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(N2CCN(c3ncnc4[nH]ccc34)CC2)cc1
Reaction #255290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1ccc2c(Cl)ncnc21
Reaction #262100
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)[Si](C(C)C)(C(C)C)n1ccc2c(Cl)ncnc21
Reaction #262971
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(S(=O)(=O)n2ccc3c(Cl)ncnc32)cc1
Reaction #279392
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCc1ccccc1)N1CCC12CCCN(c1ncnc3[nH]ccc13)C2
Reaction #283318
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1ncnc2[nH]cc(Br)c12
Reaction #290052
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Seite 1Weiter