部分構造検索

581128

N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #1695
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #1760
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2230
4,4'-[(2-oxoimidazolin-1,3-diyl) bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2794
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CN2CCN(Cc3ccc(C#N)cc3)C2=O)cc1
Reaction #2818
4,4'-[(2-oxoimidazolin-1,3-diyl)bis(methylene)]-bis(benzonitrile)
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1OCC#N
Reaction #11798
title compound
収率 102.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1OCc1nn[nH]n1
Reaction #11799
title compound
収率 14.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #43692
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3CC#N)CC1
Reaction #48124
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1cnc2sc(CNc3ccc(C#N)cc3)nc2c1)c1ccccc1
Reaction #78616
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCN(C1CCN(c3cc(C(=O)N4CCc5cc(F)ccc54)ncc3C#N)CC1)C(=O)N2
Reaction #161862
6′-(5-fluoro-2,3-dihydro-indole-1-carbonyl)-4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo-[d][1,3]diazepin-3-yl)-3,4,5,6-tetrahydro-2H-[1,4′]bipyridinyl-3′-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1C1CCN(C(=O)c2cc3cc(Cl)ccc3n2CC#N)CC1
Reaction #174120
DOI: 10.1039/C8SC04228D
CC1=C(C(=O)c2ccco2)C(c2ccc(C#N)cc2)N(CC(=O)NS(=O)(=O)CC(F)(F)F)C(=O)N1c1cccc(C(F)(F)F)c1
Reaction #175743
DOI: 10.1039/C8SC04228D
CC(C)c1cccc(C(C)C)c1NC(=O)CN1C(=O)N(c2ccc(C#N)cc2)C2(CCCCC2)C1=O
Reaction #177015
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)N2CCN(CCO)CC2)C(c2cccc(Cl)c2)C1(C#N)c1ccc(Cl)cc1
Reaction #179895
DOI: 10.1039/C8SC04228D
COc1ccc(C2C(CCC(O[Si](C)(C)C(C)(C)C)c3ccc(F)cc3)C(=O)N2c2ccc(C#N)cc2)cc1
Reaction #219927
4-[3-[3-(tert-butyidimethylsilanyloxy)-3-(4-fluorophenyl)propyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2C(CCC(O)c3ccc(F)cc3)C(=O)N2c2ccc(C#N)cc2)cc1
Reaction #219928
4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2C(CCC(O)c3ccc(F)cc3)C(=O)N2c2ccc(CN)cc2)cc1
Reaction #219929
1-(4-Aminomethylphenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-methoxyphenyl)-azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2C(CCC(O[Si](C)(C)C(C)(C)C)c3ccc(F)cc3)C(=O)N2c2ccc(C#N)cc2)cc1
Reaction #220890
4-[3-[3-(tert-butyldimethylsilanyloxy)-3-(4-fluorophenyl)propyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2C(CCC(O)c3ccc(F)cc3)C(=O)N2c2ccc(C#N)cc2)cc1
Reaction #220891
4-[3-[3-(4-Fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
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