Recherche de Sous-structure

1315575

Cc1nc(C)c(C(C)(O)c2cccnc2)s1
Reaction #2919
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NOC(=O)OC(C)(C)C)nc1C(F)(F)F
Reaction #9186
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)ONc1nc(C(F)(F)F)c(C(=O)O)s1
Reaction #9187
2-Tert-butoxycarbonyloxyamino-4-trifluoromethyl-thiazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1-c1ncc(C(C)O)s1
Reaction #69950
1-[2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethanol
Rendement 70.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1-c1ncc(C(C)OC2=CC(=O)C3C4CCC(O4)C23)s1
Reaction #69951
5-{1-[2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Rendement 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cnc(Cn3ncc([N+](=O)[O-])n3)s2)OCCO1
Reaction #71119
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cnc(Cn3ncc(N)n3)s2)OCCO1
Reaction #71120
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@@H]2CCN(c3ncc(C)s3)C[C@@H]2OC)nc1Cl
Reaction #71798
title compound
Rendement 100.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](N)C2)nc1C
Reaction #71818
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)s3)C[C@H]2OCCF)nc1Cl
Reaction #71978
title compound
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3ncc(C(=O)O)s3)C[C@H]2OCCCF)nc1Cl
Reaction #71988
title compound
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC(NC(=O)OC(C)(C)C)C2)nc1C
Reaction #72154
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC(N)C2)nc1C
Reaction #72155
title compound
Rendement 79.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(N2CC(NC(=O)OC(C)(C)C)C2)sc1C(=O)OCC
Reaction #72158
title compound
Rendement 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc(N2CC(NC(=O)OC(C)(C)C)C2)sc1C(=O)OC
Reaction #72164
title compound
Rendement 66.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc(N2CC(N)C2)sc1C(=O)OC
Reaction #72165
title compound
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C(=O)c1nc(Cl)c(CC)[nH]1)C1CN(c2nc(C)c(C(=O)OCC)s2)C1
Reaction #72188
title compound
Rendement 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-n2ncc3c2CCC(NC(=O)c2nc(Cl)c(CC)[nH]2)C3)nc1C
Reaction #72217
title compound
Rendement 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-n2cc3c(n2)CCC(NC(=O)c2nc(Cl)c(CC)[nH]2)C3)nc1C
Reaction #72218
title compound
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2nc(C(=O)NCCF)c(C(=O)O)s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72232
title compound
Rendement 41.7%DOI: 10.6084/m9.figshare.5104873.v1
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