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1436

CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)c3ccc(Cl)cc3)CC2)cc1
Reaction #1747
trans-O-(4-Chlorobenzoyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@@H](OC(=O)c3ccc(Cl)cc3)CC2)cc1
Reaction #1754
cis-O-(4-Chlorobenzoyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccc(Cl)cc1Cl
Reaction #3587
desired product
Выход 53.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1C(=O)Cl
Reaction #3609
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3610
desired product
Выход 41.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1NC(=O)c1ccc(Cl)cc1Cl
Reaction #3660
crystals
Выход 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2n1Cc1ccccc1N(C(=O)c1ccc(NC(=O)c3ccc(Cl)cc3Cl)c(C)c1)C2
Reaction #3695
solid
Выход 55.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2Cc3nccn3Cc3ccccc32)cc1)c1ccc(Cl)cc1Cl
Reaction #3701
tan foam
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2CCc3cccn3-c3ccccc32)c(Cl)c1)c1ccc(Cl)cc1Cl
Reaction #3705
white solid
Выход 99.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
Reaction #4360
diethyl (2,4-dichloro-5-fluoro-3-nitro-benzoyl)-malonate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(N3CCN(C(=O)c4cc(S(N)(=O)=O)c(Cl)cc4Cl)CC3)nc(C)n2)cc1OC
Reaction #4436
4-[4-(2,4-dichloro-5-sulfamoylbenzoyl)piperazin-1-yl]-6-(3,4-dimethoxyphenyl)-2-methylpyrimidine
Выход 71.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NCCCSc1ccncc1)c1ccc(Cl)cc1
Reaction #6200
desired compound
Выход 118.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc(Cl)cc4)c3C2=O)C(=O)N1
Reaction #10101
4-chloro-N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-benzamide
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc(C(=O)NNC(=O)c2cc(Cl)ccc2Cl)cc1
Reaction #11274
required product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCCC(C(=O)c2ccc(Cl)cc2Cl)C1=O
Reaction #40891
ethyl [3-(2,4-dichlorobenzoyl)-2-oxocyclohexyl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3ccc(Cl)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43868
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2cncc(-c3ccc(C(=O)c4ccc(Cl)cc4)cc3N)n2)cc(OC)c1OC
Reaction #44595
title compound
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)cc(Cl)c1C(=O)NC(c1ccccc1)C(C)(C)N1CCCC1
Reaction #49128
title compound
Выход 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(NC(=O)c1ccc(Cl)c(Cl)c1)c1ccccc1
Reaction #49512
3,4-dichloro-N-(1-methyl-1-phenylethyl)benzamide
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)c1ccccn1)C(=O)c1ccc(Cl)c(Cl)c1
Reaction #49926
N'-t-butyl-N-(2-pyridinecarbonyl)-N'-(3,4-dichlorobenzoyl)hydrazine
Выход 79.1%DOI: 10.6084/m9.figshare.5104873.v1
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