Busqueda de Subestructura

38460

N#CC(c1ccccc1)(c1ccccc1)C1CCCN(CCCc2ccccc2)C1
Reaction #49669
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(O)cc2)C1
Reaction #49670
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(C(N)=O)cc2)C1
Reaction #49671
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)C1CCCN(Cc2ccc3c(c2)OCO3)C1
Reaction #49672
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CCc2ccc(CN)cc2)nc2cc(C(=O)NN3CCC(NC(=O)c4ccccc4)CC3)ccc21
Reaction #52190
2-[2-(4-Aminomethylphenyl)-ethyl]-1-methyl-benzimidazole-5-yl-carboxylic acid-(4-benzamido-piperidinyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=C1CC(C)(C)NC(C)(C)C1
Reaction #54459
Ethyl 2,2,6,6-tetramethyl-4-piperidinylidene-cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)C1CC(C)(C)NC(C)(C)C1
Reaction #54460
ethyl 2-(2,2,6,6-tetramethyl-4-piperidinyl)-cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(=O)c2ccc(OCCCN3CCC(=C(c4ccccc4)c4ccccc4)CC3)cc2o1
Reaction #65477
2-cyano-7-[3-(4-diphenylmethylenepiperidin-1-yl)propyloxy]-4-oxo-4H-benzopyran
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2ncc(=O)n(CCN3CCC(NCc4cc5c(cn4)OCCO5)CC3)c2c1
Reaction #68295
1-(2-(4-((2,3-dihydro-1,4-dioxino[2,3-c]pyridin-7-yl)methylamino)piperidin-1-yl)ethyl)-7-cyanoquinoxalin-2(1H)-one
Rendimiento 49.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc2ncc(=O)n(CCN3CCC(NCc4cc5c(cn4)OCCO5)CC3)c2c1
Reaction #68296
1-(2-(4-((2,3-dihydro-1,4-dioxino[2,3-c]pyridin-7-yl)methylamino)piperidin-1-yl)ethyl)-7-cyanoquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70437
Example 48
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70438
Example 48
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #70439
Example 48
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncccc1C12CCCN(CC1)C2
Reaction #72738
expected product
Rendimiento 76.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.O
Reaction #78341
expected product
Rendimiento 105.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.Cl.NCC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.NCC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.O
Reaction #78342
expected product
Rendimiento 111.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CN(/C(=N/C#N)N2CCCCC2)CC[C@@H]1C(=O)N1CCN(c2ccc(C#N)cc2C)CC1
Reaction #89764
methyl(3R,4S)-1-[(E)-(cyanoimino)(piperidin-1-yl)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonylpiperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1N1CCN(C(=O)[C@H]2CCN(/C(=N/C#N)N3CCCCC3)C[C@@H]2C(=O)NO)CC1
Reaction #89765
(3R,4S)-1-[(E)-(cyanoimino)(piperidin-1-yl)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonyl-N-hydroxypiperidine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c[nH]c2ccc(CCNC(=O)c3ccc(-c4ccnc(NCCCCCN5CCCCC5)n4)cc3)cc12
Reaction #179298
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-n2cc(Cl)c(OC3CCNCC3)cc2=O)cc1F
Reaction #183710
DOI: 10.1039/C8SC04228D
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