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CCN(CC)C=O

COc1cc2c(Cl)cnnc2cc1OCc1ccncc1.Cl
Reaction #7572
4-chloro-6-methoxy-7-(4-pyridylmethoxy)cinnoline hydrochloride
Ausbeute 122.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(N2CCOCC2)c(F)c1
Reaction #8238
oil
Ausbeute 331.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8240
solid
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2ccnc2)c(F)c1
Reaction #8243
desired product
Ausbeute 158.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8245
desired product
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nn3c(c2-c2ccnc4ccccc24)OCC3)nc1
Reaction #8376
title compound
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(SCC=C(c2ccc(-c3cccnc3)cc2)c2ccc(-c3cccnc3)cc2)cc1C(F)(F)F
Reaction #9440
{4-[3,3-bis-(4-pyridin-3-yl-phenyl)-allylsulfanyl]-2-trifluoromethyl-phenoxy}-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CNc1ccc(OC(F)(F)F)cc1)NC(=O)[C@H](CSCc1ccccc1)NC(=O)N1CCOCC1
Reaction #43553
off-white solid
Ausbeute 6.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CNc1ccc(OC(F)(F)F)cc1)NC(=O)[C@H](CCC1CCCCC1)CC(=O)N1CCOCC1
Reaction #43557
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(COc3ccc4c(c3)OC[C@H]4CC(=O)OC)c2)c(C)c1
Reaction #43918
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4COC(C)=O)c3)ccc21
Reaction #43930
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCCCOc1cc(C)c(Br)c(C)c1
Reaction #43938
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OC5CCS(=O)(=O)CC5)cc4C)c3)ccc21
Reaction #43943
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(C)c(OCCCS(C)(=O)=O)c(C)c4C)c3)ccc21
Reaction #43946
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4C)c3)ccc21
Reaction #43948
title compound
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)c(F)c4C)c3)ccc21
Reaction #43951
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)c(Cl)c(OCCCS(C)(=O)=O)c(Cl)c4C)c3)ccc21
Reaction #43960
title compound
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OCCCS(C)(=O)=O)cc(CC)c1-c1cccc(COc2ccc3c(c2)OC[C@H]3CC(=O)OC)c1
Reaction #43962
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cc1cccc(Br)n1
Reaction #45378
2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(O)c(=O)n1CCCCCl)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46270
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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