Ähnlichkeitssuche

51453

Cc1c(-c2ccccc2)c(F)c2oc(C(=O)N3CCCCC3)nc2c1C#N
Reaction #45657
compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(c(N3CC[C@H](N(C)C)C3)c1-c1ccccc1)OC(C#N)(C(=O)N1CCCCC1)N2
Reaction #45658
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CCC3)nc2c1C#N
Reaction #45683
solid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CCC3)nc2c1C#N
Reaction #45684
solid
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CCCC3)nc2c1C#N
Reaction #45685
oil
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CCCC3)nc2c1C#N
Reaction #45686
solid
Ausbeute 29.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CCCCC3)nc2c1C#N
Reaction #45687
solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CCCCC3)nc2c1C#N
Reaction #45688
solid
Ausbeute 44.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CC(O)C3)nc2c1C#N
Reaction #45696
7-Fluoro-2-(3-hydroxyazetidin-1-yl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CC(O)C3)nc2c1C#N
Reaction #45697
compound
Ausbeute 23.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CC(C(=O)N(C)C)C3)nc2c1C#N
Reaction #45699
oil
Ausbeute 86.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)C1
Reaction #45700
Ethyl 1-(4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazol-2-yl)azetidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)CC1
Reaction #45706
oil
Ausbeute 94.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(N4CC[C@H](N(C)C)C4)c3o2)CC1
Reaction #45707
Ethyl 1-{4-cyano-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazol-2-yl}piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CCN(C)C(=O)C3)nc2c1C#N
Reaction #45752
compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CCN(C)C(=O)C3)nc2c1C#N
Reaction #45753
compound
Ausbeute 57.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)C1
Reaction #45756
compound
Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CN(c2nc3c(C#N)c(C)c(-c4ccccc4)c(N4CC[C@H](N(C)C)C4)c3o2)C1
Reaction #45757
compound
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(F)c2oc(N3CC(CO)C3)nc2c1C#N
Reaction #45759
compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(N3CC(CO)C3)nc2c1C#N
Reaction #45760
compound
Ausbeute 130.3%DOI: 10.6084/m9.figshare.5104873.v1
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