Поиск подструктуры

915

O=C(O)c1cnn(C2CCOCC2)c1Cl
Reaction #41162
5-chloro-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid
Выход 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1COCC[C@H]1N1CCCC1
Reaction #67699
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1COCCC1N1CCCC1
Reaction #67700
4-Pyrrolidin-1-yl-tetrahydro-pyran-3-ylamine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1COCC[C@H]1NC1CCCC1
Reaction #67704
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)C2CCOCC2)c2sc(N)nc12
Reaction #80178
4-methoxy-N7-methyl-N7-(tetrahydro-pyran-4-yl)-benzothiazole-2,7-diamine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)C2CCOCC2)c2sc(NC(=O)c3ccnc(Br)c3)nc12
Reaction #80179
2-bromo-N-{4-methoxy-7-[methyl-(tetrahydro-pyran-4-yl)-amino]-benzothiazol-2-yl}-isonicotinamide
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1C[C@H](NC(=O)OC(C)(C)C)[C@H](N)CO1
Reaction #84724
title compound
Выход 18.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1cccc(-c2nc(Nc3ccc4[nH]ncc4c3)c3ccccc3n2)c1)NC1CCOCC1
Reaction #89869
2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(tetrahydro-2H-pyran-4-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(NC(=O)OC(C)(C)C)CCOCC1
Reaction #165924
title compound
Выход 31.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](/C=C/C(=O)N1CCc2ccccc21)NC(=O)C1(N)CCOCC1.Cl
Reaction #165926
title compound
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CC(=O)O)C1CCOCC1
Reaction #167560
2-(tert-butoxycarbonyl(tetrahydro-2H-pyran-4-yl)amino)acetic acid
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(=O)N[C@H]2CCOC[C@@H]2O)cc(Br)c2ccccc12
Reaction #169622
1-amino-4-bromo-N-[(3R,4S)-3-hydroxytetrahydro-2H-pyran-4-yl]-2-naphthamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC1CCOCC1)C(=O)O
Reaction #173123
DOI: 10.1039/C8SC04228D
O=S1(=O)CCN(CCc2cccc(-c3cc4cc(Cl)cc(NC5CCOCC5)c4[nH]3)c2)CC1
Reaction #174935
DOI: 10.1039/C8SC04228D
Clc1cc(NC2CCOCC2)c2[nH]cc(-c3ccccc3)c2c1
Reaction #187192
DOI: 10.1039/C8SC04228D
Clc1ccc(CNC2CCC(C(c3ccccc3)c3ccccc3)OC2)cc1Cl
Reaction #188663
DOI: 10.1039/C8SC04228D
CCN(c1cc(-c2ccc(CN3CCOCC3)cc2)cc(C(=O)NCc2c(C)c(F)c(C)[nH]c2=O)c1C)C1CCOCC1
Reaction #191096
DOI: 10.1039/C8SC04228D
Nc1c(F)c(F)cc2c1c(=O)c(C(=O)O)cn2C1CCOCC1
Reaction #191273
DOI: 10.1039/C8SC04228D
CC1COCCC1Nc1nc(Cl)ncc1[N+](=O)[O-]
Reaction #206382
DOI: 10.1039/C8SC04228D
N#Cc1ccc(CNC2CCC(C(c3ccccc3)c3ccccc3)OC2)cc1
Reaction #210704
DOI: 10.1039/C8SC04228D
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