部分構造検索

CCOc1ccccn1

CS(=O)(=O)N1CCC(Oc2cccc3ncc([N+](=O)[O-])n23)CC1
Reaction #5571
desired product
収率 54.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(Oc2cccc3ncc(N)n23)CC1
Reaction #5572
desired product
収率 132.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #11812
title compound
収率 89.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ncc(Cl)cc1N
Reaction #11813
title compound
収率 92.8%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1cnc(OCc2ccccc2)cc1C#Cc1ccc(F)cc1
Reaction #72340
2-(benzyloxy)-4-((4-fluorophenyl)ethynyl)-5-(methoxymethoxy)pyridine
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cnc(OCc2ccccc2)cc1C#Cc1ccc(F)cc1
Reaction #72341
6-(benzyloxy)-4-((4-fluorophenyl)ethynyl)pyridin-3-ol
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(Oc2ccc3c4cc(C#N)ncc4n(COCC[Si](C)(C)C)c3n2)CCCNC1
Reaction #88559
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(/C=C/c2cnc(OCCOCCOCCF)c(Br)c2)cc1
Reaction #164430
11e
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(OCCN)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12.Cl.Cl
Reaction #166464
N-(1-((6-(2-aminoethoxy)pyridin-2-yl)methyl)-3-ethyl-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide dihydrochloride
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(OCCCN)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12.Cl.Cl
Reaction #166466
N-(1-((6-(3-aminopropoxy)pyridin-2-yl)methyl)-3-ethyl-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(OC[C@@H]3[C@@H](O)CCN3C)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166527
final product
収率 77.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(OCC(O)CO)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12.Cl.Cl
Reaction #166591
N-(1-((6-(2,3-dihydroxypropoxy)pyridin-2-yl)methyl)-3-ethyl-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide dihydrochloride
収率 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncc(C(=O)c2cn(C(C)C)c3ncncc23)cc1NC(=O)Cn1nc(C(F)(F)F)cc1C
Reaction #169309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ncc(C(=O)c2cn(C(C)C)c3ncncc23)cc1N
Reaction #169451
title compound
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCc2cccc(N3CCN(CCCCOc4ccc5ccc(=O)[nH]c5n4)CC3)c21
Reaction #182942
DOI: 10.1039/C8SC04228D
Oc1ccc(C=Cc2cnc(OCCOCCOCCF)c(Br)c2)cc1
Reaction #189661
DOI: 10.1039/C8SC04228D
Cc1nc(C(C)(CC2CC2)NC(=O)c2ccc(N3CC(F)(F)C3)c(OCC3CC3)n2)no1
Reaction #193098
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cn(Cc2ccc(OCc3nc(-c4ccccc4)oc3C)nc2)cc1-c1ccccc1
Reaction #198695
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N1CCC(Oc2cccc3ncc([N+](=O)[O-])n23)CC1
Reaction #201825
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(Cl)cn1)C1CCN(Cc2ccccc2)CC1c1ccc(Cl)cc1
Reaction #202733
DOI: 10.1039/C8SC04228D
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