子结构搜索

Cc1ccc(O)c(C(N)=O)c1

COCCOc1ccc(OCC(O)CNCCCc2ccc(O)c(C(N)=O)c2)cc1
Reaction #4623
1-[3-(3-carbamoyl-4-hydroxyphenyl)propylamino]-3-[4-(2-methoxyethoxy)phenoxy]propan-2-ol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50235
solid
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc([N+](=O)[O-])cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69702
(2,4-bis-benzyloxy-5-isopropyl-phenyl)-(5-nitro-1,3-dihydro-isoindol-2-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc(N)cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69703
(5-amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanone
收率 87.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc(C(=O)N4CCN(C(=O)OC(C)(C)C)CC4)cc3C2)c(O)cc1O
Reaction #69728
4-[2-(2,4-dihydroxy-5-isopropyl-benzoyl)-2,3-dihydro-1H-isoindole-5-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1/c(=N/C(=O)c2cc(C(F)(F)F)ccc2OC[C@H](C)O)sc2ccncc21
Reaction #71570
title compound
收率 19.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77802
5-formyl-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77803
aimed product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC#N)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77804
5-cyanomethyl-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(N)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77805
5-carbamoylmethyl-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(C(=O)O)S(C)(=O)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77814
aimed product
收率 74.9%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(C(=O)CCCCN2CCN(c3ccccc3)CC2)ccc1OCc1ccccc1
Reaction #93486
5-[5-(4-phenyl-1-piperazinyl)valeryl]-2-benzyloxy-benzamide
收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1C=C(C(=O)CCCN2CCN(c3ccccc3)CC2)C=CC1(O)OCc1ccccc1
Reaction #93488
5-[4-(4-phenyl-1-piperazinyl)butyryl]-2-benzyloxy-salicylamide
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cn(C(C)(C)C)s/c1=N\C(=O)c1cc(C=O)ccc1OC
Reaction #163446
title compound
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(OC)c(C(=O)/N=c2\sn(C(C)(C)C)cc2CCCC)c1
Reaction #163448
title compound
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cn(C(C)(C)C)s/c1=N\C(=O)c1cc(C(N)=O)ccc1OC
Reaction #163451
title compound
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(N2CCC(CCS(C)(=O)=O)CC2)c(CC)cc1Nc1nccc(-c2c(-c3ccc(OCC)c(C(=O)Nc4c(F)cccc4F)c3)nc3ccccn23)n1
Reaction #180545
DOI: 10.1039/C8SC04228D
CCCCc1cn(C(C)(C)C)sc1=NC(=O)c1cc(C(N)=O)ccc1OC
Reaction #189017
DOI: 10.1039/C8SC04228D
COCOc1ccc(CN2CCN(C)CC2)cc1C(=O)Nc1cc(-c2ccccc2)ccc1C(=O)OC(C)(C)C
Reaction #190721
DOI: 10.1039/C8SC04228D
CC(C)(C)NCC(O)c1ccc(OCc2ccccc2)c(C(N)=O)c1
Reaction #191966
DOI: 10.1039/C8SC04228D
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