Busqueda de Subestructura

184338

Cc1nc2cc([N+](=O)[O-])ccc2o1
Reaction #5601
5-nitro-2-methylbenzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)c(C2=CC(NC(=O)OC(C)(C)C)CC2)c2oc(C(C)(C)C)nc2c1C#N
Reaction #45546
tert-butyl [3-(2-tert-butyl-4-cyano-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)-2-cyclopentenyl]carbamate
Rendimiento 61.0%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
Rendimiento 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
Rendimiento 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
COCCN(C)C(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45664
compound
Rendimiento 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
Rendimiento 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
Rendimiento 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
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(-c3nc(C(=O)O)cs3)nc2c1C#N
Reaction #45770
compound
Rendimiento 61.0%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
Rendimiento 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
Rendimiento 11.1%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
Rendimiento 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
Rendimiento 32.2%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(c2c(-c3ccccc3)c(C)c(C#N)c3nc(C4CC4)oc23)C1
Reaction #45856
compound
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@H]1CCN(c2c(-c3ccccc3)c(C)c(C#N)c3nc(C4CC4)oc23)C1
Reaction #45857
compound
Rendimiento 23.5%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(c2c(-c3ccccc3)c(CF)c(C#N)c3nc(C4CC4)oc23)C1
Reaction #45860
compound
Rendimiento 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente