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1049816

COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4cc(F)ccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #199759
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #424246
subtitle product
収率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #424267
subtitle product
収率 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4ccccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #424272
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4cc(F)ccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #424300
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(N[C@@H](c3ccccc3)[C@@H](C)CO)c2=O)c1
Reaction #424345
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3SCCOCc3ccccc3)c2=O)c1
Reaction #893008
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4ccccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #956989
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4ccccc4OCCNCC(=O)OCc4ccccc4)CC3)c2=O)c1
Reaction #956997
methyl 3-[3-[1-[2-[2-[(benzyloxycarbonyl)methylamino]ethoxy]phenyl]cyclopropylamino]-5-bromo-2-oxo-1(2H)-pyrazinyl]-5-fluoro-4-methylbenzoate
収率 164.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cc(C(=O)NC2CC2)cc1-n1cc(Br)nc(NC2(c3ccccc3OCCN(C)C(=O)OCc3ccccc3)CC2)c1=O
Reaction #956999
benzyl [2-[2-[1-[[6-bromo-4-[5-(cyclopropylcarbamoyl)-3-fluoro-2-methylphenyl]-3-oxo-3,4-dihydro-2-pyrazinyl]amino]cyclopropyl]phenoxy]ethyl]methylcarbamate
収率 3.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(c3ccccc3)C(C)CO)c2=O)c1
Reaction #1314596
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #1784505
subtitle product
収率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #1784527
subtitle product
収率 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4ccccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #1784532
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4cc(F)ccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #1784559
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(N[C@@H](c3ccccc3)[C@@H](C)CO)c2=O)c1
Reaction #1784603
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #2157924
subtitle product
収率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC(C)(C)c3ccccc3OCc3ccccc3)c2=O)c1
Reaction #2157944
subtitle product
収率 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4ccccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #2157948
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)c(C)c(-n2cc(Br)nc(NC3(c4cc(F)ccc4OCc4ccccc4)CC3)c2=O)c1
Reaction #2157976
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
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