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2330

CCN(CCCOC)C(=N)N
Reaction #859
title compound
Ausbeute 50.0%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
CN1CCN(C2c3cc(C#N)ccc3OC(C)(C)C2O)C1=NC#N
Reaction #240780
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(N2CCCNC2=NC#N)c2cc(C#N)ccc2OC1(C)C
Reaction #278910
DOI: 10.1039/C8SC04228D
CCC(=O)N1CCCN(CC2CCOC2)C1=N[N+](=O)[O-]
Reaction #295865
DOI: 10.1039/C8SC04228D
CC(=O)N(C1=NC2C(C=N1)C=C(Oc1ccc(F)cc1F)C(=O)N2C)C1CCOCC1
Reaction #357912
N-[6-(2,4-Difluoro-phenoxy)-8-methyl-7-oxo-4a,7,8,8a-tetrahydro-pyrido[2,3 d]pyrimidin-2-yl]-N-(tetrahydro-pyran-4-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2C(N2CCNC2=NC#N)C1O
Reaction #372645
DOI: 10.1039/C8SC04228D
COC(=O)NCCOC(c1cccc(Cl)c1)C1CCCN(C(=NC#N)NC(CC2CCCCC2)CN(C)C(=O)OC(C)(C)C)C1
Reaction #408987
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CC(CO)N(Cc3ccc(OC)c(OC)c3)C2=Nc2c(Cl)cccc2Cl)cc1OC
Reaction #417707
( 9 )
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(COCC(O)CNC(C)(C)C)N(Cc3ccc(OC)c(OC)c3)C2=Nc2c(Cl)cccc2Cl)cc1OC
Reaction #417708
( 10 )
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCNC2=NC#N)[C@@H]1O
Reaction #431955
title compound
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NCCO[C@@H](c1cccc(Cl)c1)[C@@H]1CCCN(C(=NC#N)N[C@@H](CC2CCCCC2)CN(C)C(=O)OC(C)(C)C)C1
Reaction #539082
methyl 2-((R)-(3-chlorophenyl)((R)-1-(N′-cyano-N—((S)-1-cyclohexyl-3-(N-methyl-N-(tert-butoxycarbonyl)amino)propan-2-yl)carbamimidoyl)piperidin-3-yl)methoxy)ethylcarbamate
Ausbeute 2.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@H](CC1CCCCC1)NC(=NC#N)N1CCC[C@@H]([C@@H](OCCNC(=O)OC)c2cccc(Cl)c2)C1
Reaction #539083
product
Ausbeute 59.0%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 #622276
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 #622277
(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
NC(=NO)N1CCC(Oc2cc(F)ccc2Br)CC1
Reaction #648396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Br)c(OC2CCN(c3noc(-c4cc[nH]c4)n3)CC2)c1
Reaction #648397
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCCOC)C(=N)N
Reaction #722732
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(CC(=O)O)N2CCN(CCCc3ccc4c(n3)NCCC4)C2=NC#N)cn1
Reaction #757795
DOI: 10.1039/C8SC04228D
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