#16506821

CCOC(=O)CNC(=O)c1c(O)c2cc(C#N)ccc2n(C)c1=O
Reaction #41923
ethyl 2-(6-cyano-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nn(-c2ccnc3[nH]ccc23)cc1/C=C/C#N
Reaction #69156
product
収率 191.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nn(-c2ccnc3[nH]ccc23)cc1/C=C/C#N
Reaction #73188
product
収率 191.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC=Cc1cc(-c2ccccc2)c2nncn2c1
Reaction #175975
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC=CC=CC(=O)OCC1CO1
Reaction #189196
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC1=CCCCC1
Reaction #191010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1OC(Cl)C(N=[N+]=[N-])C(OC(C)=O)C1OC(C)=O
Reaction #198983
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(C)c1NCC1COCO1
Reaction #201519
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nccc1Cc1ccc(Sc2cccc(C3(C(N)=O)CCOCC3)c2)cc1F
Reaction #204797
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)C1(c2cccc(Sc3ccc(Br)cc3Cl)c2)CCOCC1
Reaction #210004
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(=O)OC(C)C)c(C(=O)c2ccccc2C#N)cc1OCc1ccccc1
Reaction #221261
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCC(Cl)C(=O)O
Reaction #225348
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(C=Cc1ccccc1)OCC1CO1
Reaction #229107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(I)c(O)c(C=O)c1
Reaction #231061
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1nc2n(n1)CCOc1cc(Cl)ccc1-2
Reaction #235574
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1ccc2c(n1)-c1sccc1CCO2
Reaction #241788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(C)c1NCC1COCO1
Reaction #245949
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1CN(C(=O)OC(C)(C)C)CC2Cc3ccc(C#N)cc3N12
Reaction #247665
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Nc1nc(Cl)c2ncn(COC(COC(=O)C(C)(C)C)COC(=O)C(C)(C)C)c2n1
Reaction #249721
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(C=CC=Cc1ccccc1)OCC1CO1
Reaction #259912
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
1 ページ次のページ