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15740

NCC(O)C[n+]1ccc(SCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)CSc4cc(Cl)ccc4Cl)[C@H]3SC2)cc1.[Cl-]
Reaction #3762
title compound
수율 127.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)c3ccc(Br)cc3)CS[C@H]12
Reaction #5643
title compound
수율 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=NC#N)NCCCSc1nccc(NC(N)=NCC(F)(F)F)n1
Reaction #63072
4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[3-(2-cyano-3-[2-diethylaminoethyl]guanidino)propylthio]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Sc2c[nH]c3ccc(C#N)cc23)CC1
Reaction #65168
3-[(1-methylpiperidin-4-yl)thio]-1H-indole-5-carbonitrile
수율 5.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Sc2c[nH]c3ccc(O)cc23)CC1
Reaction #65169
3-[(1-methylpiperidin-4-yl)thio]-1H-indol-5-ol
수율 10.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1cc(SC2CCN(C)CC2)c2cc(Br)ccc21
Reaction #65175
5-bromo-1-butyl-3-[(1-methylpiperidin-4-yl)thio]1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)c3ccc(Br)cc3)CS[C@H]12
Reaction #65629
title compound
수율 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cccc(-c2nn3c(c2-c2ccncc2)SCCC3)c1)c1cccc(F)c1
Reaction #66356
3-fluoro-N-[3-(3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]thiazin-2-yl)-phenyl]-benzenesulfonamide
수율 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #66358
solid
수율 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(C(=O)N2C[C@H](S(=O)(=O)c3ccccc3Cl)C[C@H]2C(=O)NC2(C#N)CC2)(c2ncc(Br)cc2F)C1
Reaction #156711
title compound
수율 40.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CCSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157631
title compound
수율 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CSc3ccccc3N(CC(=O)O)C2=O)cc1
Reaction #178462
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(S(=O)(=O)N2CCC(S(=O)c3cc(C(C)(C)C)c(O)c(C(C)(C)C)c3)CC2)n1C
Reaction #194618
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)C2(C(=O)O)CCN(CCCc3ccccc3)CC2)cc1
Reaction #196008
DOI: 10.1039/C8SC04228D
O=C(O)CN1CC(c2ccccc2)SCC(NC(CCc2ccccc2)C(=O)O)C1=O
Reaction #225151
DOI: 10.1039/C8SC04228D
CNCCN1C(=O)C(O)C(c2ccc(OC)cc2)Sc2cc(Cl)ccc21
Reaction #228401
DOI: 10.1039/C8SC04228D
CS(=O)(=O)C1CCN(Cc2cc3c(N4CCOCC4)nc(-c4cnc(N)nc4)nc3s2)CC1
Reaction #230834
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)OCc1ccccc1)C(=O)OC(C)(C)CN1CCOCC1
Reaction #234183
DOI: 10.1039/C8SC04228D
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