Teilstruktursuche

1424009

Cc1nc(Cl)ncc1Br
Reaction #62365
title compound
Ausbeute 35.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(C(F)(F)F)cc2)c(CCCO)o1
Reaction #76212
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(Cl)c(Cl)c2)c(CCCO)o1
Reaction #76218
title compound
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)CO)c(O)cc1NC(=O)c1c[nH]c2ccccc2c1=O
Reaction #163972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=N)c1c(Cl)cc2c3c(cccc13)COC2
Reaction #304481
1-(5-chloro-1H,3H-benzo[de]isochromen-6-yl)-ethylidene-amine
Ausbeute 102.8%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cnc(N[C@@H]2CCCN(CC3CCCCC3)C2)c(Cl)c1
Reaction #313626
(5-chloro-6-{[(3R)-1-(cyclohexylmethyl)-3-piperidinyl]amino}-3-pyridinyl)methanol
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(Oc2cc(CO)cc3ccc(Br)cc23)nc1
Reaction #325816
[6-bromo-4-(5-ethanesulfonyl-pyridin-2-yloxy)-naphthalen-2-yl]-methanol
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2c(CO)c(Br)nc3cc4c(cc23)OCCO4)CC1
Reaction #444703
[7-bromo-9-(4-methyl-piperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-yl]-methanol
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(C(F)(F)F)cc2)c(CCCO)o1
Reaction #482829
2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropanol
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(Cl)c(Cl)c2)c(CCCO)o1
Reaction #482830
4-(3,4-dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(CO)c1
Reaction #486661
4-methoxypyrid-2-ylmethanol
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2c(CO)c(Br)nc3cc4c(cc23)OCCO4)CC1
Reaction #499027
[7-bromo-9-(4-methyl-piperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-yl]-methanol
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1ccc2c(c1)Oc1c(Br)cccc1C2=C1CC2CCC(C1)N2
Reaction #512478
Compound 7j
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(C)(C)CO)c(O)cc1NC(=O)c1c[nH]c2ccccc2c1=O
Reaction #533326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Cn2cnc(CNC3CCCCC3)n2)cc1
Reaction #579077
(1-benzyl-1H-[1,2,4]triazol-3-ylmethyl)-cyclohexyl-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(C(F)(F)F)cc2)c(CCCO)o1
Reaction #650280
2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropanol
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1nc(-c2ccc(Cl)c(Cl)c2)c(CCCO)o1
Reaction #650281
4-(3,4-dichlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(CO)c(OC)c1
Reaction #690014
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncccc1CN1CCC(CO)(CCc2ccccc2)CC1
Reaction #693386
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Br)cnc1C(F)(F)F
Reaction #711128
product ( 29 )
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
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