子结构搜索

1230285

CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=NC#N)Oc2ccccc2)C1=O
Reaction #48445
title compound
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1-c1nc(NCCN=C(NC#N)Oc2ccccc2)nc2c1ccc(=O)n2-c1c(F)cccc1F
Reaction #58361
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#CNC(=NCCNc1nc(-c2ccc(F)cc2F)c2ccc(=O)n(-c3ccccc3F)c2n1)Oc1ccccc1
Reaction #58363
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1nc(NCCNC(=N)NC#N)nc2c1ccc(=O)n2-c1c(F)cccc1F
Reaction #58366
title compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(Oc1ccccc1)N1CCCCC1
Reaction #83648
[phenoxy(1-piperidinyl)methylene]cyanamide
收率 81.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CN(/C(=N/C#N)Oc2ccccc2)CC[C@@H]1C(=O)N1CC[C@H](c2ccccc2)C1
Reaction #89758
product
收率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CN(/C(=N/C#N)Oc2ccccc2)CC[C@@H]1C(=O)N1CCN(c2ccc(C#N)cc2C)CC1
Reaction #89763
methyl(3R,4S)-1-[(Z)-(cyanoimino)(phenoxy)methyl]-4-[4-(4-cyano-2-methylphenyl)piperazin-1-yl]carbonylpiperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(N[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(CC(F)(F)F)C1=O)N1CCC(c2cc3ccccc3[nH]c2=O)CC1
Reaction #219684
Title compound
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(N[C@@H]1Cc2cc(Cl)c3[nH]ncc3c2CN(CC(F)(F)F)C1=O)N1CCC(c2cc3cccc(F)c3[nH]c2=O)CC1
Reaction #219685
Title compound
收率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc2ncnc(N)c2c1-c1ccc(NC(=NC#N)Oc2ccccc2)cc1
Reaction #314805
desired product
收率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(Nc1cc(Cl)cc(N=[N+]=[N-])c1)Oc1ccccc1
Reaction #347345
N-(3-azido-5-chlorophenyl)-N'-cyanocarbamimidic acid, phenyl ester
收率 61.8%DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(Nc1cc(I)cc(N=[N+]=[N-])c1)Oc1ccccc1
Reaction #347350
N-(3-azido-5-iodophenyl)-N'-cyanocarbamimidic acid, phenyl ester
收率 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=NC#N)Oc2ccccc2)C1=O
Reaction #359137
title compound
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(Oc1ccccc1)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #430516
title compound
收率 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N=C(NC#N)Oc2ccccc2)c1
Reaction #482555
N-Cyano-N′-3-methoxyphenylcarbamimidic Acid, Phenyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
N#C/N=C(/Nc1ccc(OCCN2CCCC2)cc1)Oc1ccccc1
Reaction #487595
(Z)-phenyl N′-cyano-N-(4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)carbamimidate
DOI: 10.6084/m9.figshare.5104873.v1
N#CN=C(NCC#Cc1ccc2ncnc(Nc3ccc4c(cnn4Cc4cccc(F)c4)c3)c2c1)Oc1ccccc1
Reaction #502208
pure desired product
收率 49.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)NCc1cccc(F)c1Cl)[C@@H](CCCN/C(=N/C#N)Oc1ccccc1)COC(=O)Nc1cc2cc(F)ccc2cn1
Reaction #503570
(S,Z)-2-(3-(2-chloro-3-fluorobenzyl)-1-methylureido)-5-((cyanoimino)(phenoxy)methylamino)pentyl 6-fluoroisoquinolin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)CNC(=NC#N)Oc2ccccc2)nc1OC1CCCC1
Reaction #518252
(±)-phenyl N′-cyano-N-[2-[6-(cyclopentyloxy)-5-methoxy-2-pyridinyl]propyl]carbamimidate
收率 61.7%DOI: 10.6084/m9.figshare.5104873.v1
N#C/N=C(/Nc1ccc(F)c(F)c1)Oc1ccccc1
Reaction #538709
title compound
收率 86.4%DOI: 10.6084/m9.figshare.5104873.v1
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