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1152419

Cc1ncc(F)c(Cl)c1Br
Reaction #1956
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cnc(Cl)c(F)c1
Reaction #88512
title compound
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCOC2CCCCO2)c(=O)c2cc(Oc3cncc(F)c3)cnc21
Reaction #88700
6-((5-fluoropyridin-3-yl)oxy)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy) propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione
Выход 38.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnco2)cc1)N(C1CC1)C1CCN(c2ncc(Br)cc2F)CC1
Reaction #156048
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)c(F)c1
Reaction #156050
N-Cyclopropyl-N-(3′-fluoro-5′-methyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-4-oxazol-5-yl-benzamide
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
Выход 40.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(c2cncc(F)c2)CCN1c1ccc2ccccc2c1
Reaction #167288
product
Выход 57.3%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cncc(NC2CCC2)c1
Reaction #177503
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ccc(-c2cnc(OCCCCCCCC)c(F)c2)cc1
Reaction #179219
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)N1CCC(ON=C2CCN(c3ncc(Br)cc3F)CC2)CC1
Reaction #184555
DOI: 10.1039/C8SC04228D
COc1ncc(F)cc1-c1ccc(C(C)=O)cc1
Reaction #190373
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-c2cncc(F)c2C=O)cc1Cl
Reaction #196633
DOI: 10.1039/C8SC04228D
Fc1cncc(-c2ccncc2)c1
Reaction #207950
DOI: 10.1039/C8SC04228D
CCCCCCCCOc1ncc(Br)cc1F
Reaction #211225
DOI: 10.1039/C8SC04228D
Fc1cc(Br)cnc1Br
Reaction #227504
DOI: 10.1039/C8SC04228D
CNc1ncc(Br)cc1F
Reaction #229661
DOI: 10.1039/C8SC04228D
O=C(O)c1ncc(Br)cc1F
Reaction #243964
DOI: 10.1039/C8SC04228D
CC#CC1CN(S(=O)(=O)c2cnc(Cl)c(F)c2)CCN1c1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #244665
DOI: 10.1039/C8SC04228D
Brc1cncc(Oc2cncnc2)c1
Reaction #248496
DOI: 10.1039/C8SC04228D
Fc1cncc(SCc2ccccc2)c1
Reaction #276327
DOI: 10.1039/C8SC04228D
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