Substructure Search

2074

—
Reaction #2869
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c(C)c(C#N)c3nc(C(C)(C)C)oc3c2N2CC[C@H](N(C)C)C2)c1
Reaction #45560
compound
Yield 2.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(O)c2)c(N2CC[C@H](N(C)C)C2)c2oc(C(C)(C)C)nc2c1C#N
Reaction #45561
2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-(3-hydroxyphenyl)-5-methyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45646
compound
Yield 7.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(C(C)(C)O)nc2c1C#N
Reaction #45647
compound
Yield 93.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45649
4-Cyano-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-N,5-dimethyl-6-phenyl-1,3-benzoxazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45651
4-Cyano-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-N,N,5-trimethyl-6-phenyl-1,3-benzoxazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(c2c(-c3ccccc3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)C1
Reaction #45652
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@@H](N(C)C)C2)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45653
compound
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCN(c2c(-c3ccccc3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)C1
Reaction #45654
4-Cyano-N,N,5-trimethyl-7-[(3R)-3-(methylamino)pyrrolidin-1-yl]-6-phenyl-1,3-benzoxazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c2c(c(N3CC[C@H](N(C)C)C3)c1-c1ccccc1)OCN2C(=O)N1CCOCC1
Reaction #45660
compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)C(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45664
compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(C(=O)N(C)CCO)nc2c1C#N
Reaction #45667
compound
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45725
product
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(c2c(-c3cccc(F)c3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)C1
Reaction #45745
4-Cyano-6-(3-fluorophenyl)-N,N,5-trimethyl-7-[(3S)-3-methylaminopyrrolidin-1-yl]-1,3-benzoxazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(N(C)C(=O)c2nc3c(C#N)c(C)c(-c4ccccc4)c(N4CC[C@H](N(C)C)C4)c3o2)C1
Reaction #45775
compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(CO)nc2c1C#N
Reaction #45789
compound
Yield 11.1%DOI: 10.6084/m9.figshare.5104873.v1
C1=CCCC1.Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2ocnc2c1C#N
Reaction #45841
compound
Yield 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45851
compound
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)C(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](NC)C3)c2o1
Reaction #45854
compound
Yield 32.2%DOI: 10.6084/m9.figshare.5104873.v1
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