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694463

CCOC(=O)Cn1ccnc(Br)c1=O
Reaction #249435
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1ccnc(NC(CN=[N+]=[N-])Cc2ccccc2)c1=O
Reaction #258177
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1ccnc(NCCCN(CC2CC2)C(=O)OC(C)(C)C)c1=O
Reaction #276204
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #397284
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1c(C)cnc(Nc2cccnc2CC)c1=O
Reaction #485570
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccnc(N[C@@H]2COC[C@H]2OCC2CC2)c1=O
Reaction #485574
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccnc(N[C@@H]2CN(C(=O)OC(C)(C)C)C[C@H]2c2ccccn2)c1=O
Reaction #485583
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(NCC(F)(F)c2ccccc2)c1=O
Reaction #886973
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #936197
7-4
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(NCC(F)(F)c2ccccc2)c1=O
Reaction #936199
7-7
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccnc(NC2COCC2OCC2CC2)c1=O
Reaction #1032284
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #1077893
2-5
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #1103442
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(NCC(F)(F)c2ccccc2)c1=O
Reaction #1103444
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #1301329
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1ccnc(Br)c1=O
Reaction #1882471
(3-Bromo-2-oxo-2H-pyrazin-1-yl)-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccnc(NCCCN(CC2CC2)C(=O)OC(C)(C)C)c1=O
Reaction #1882477
{3-[3-(tert-butoxycarbonyl-cyclopropylmethyl-amino)-propylamino]-2-oxo-2H-pyrazin-1-yl}-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1ccnc(N[C@H](CN=[N+]=[N-])Cc2ccccc2)c1=O
Reaction #1882481
(S)-[3-(1-azidomethyl-2-phenylethylamino)-2-oxo-2H-pyrazin-1-yl]-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(Br)c1=O
Reaction #1882980
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cn1c(C)cnc(NCC(F)(F)c2ccccc2)c1=O
Reaction #1882982
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
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