部分構造検索

625177

CCCCC(NC(=O)c1cccnc1-n1cc(-c2ccccc2)cn1)C(=O)C(N)=O
Reaction #40707
title compound
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(NC(=O)c1cccnc1-n1ccc(-c2ccccc2)n1)C(=O)C(N)=O
Reaction #40708
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(-c2c[nH]cn2)cc1
Reaction #385885
DOI: 10.1039/C8SC04228D
CCc1cc(-c2cncc(C(=O)NCC(=O)c3ccccc3)c2)c(C)[nH]c1=O
Reaction #390856
DOI: 10.1039/C8SC04228D
CC(=O)CNC(=O)c1cccnc1
Reaction #408655
DOI: 10.1039/C8SC04228D
O=C(NC1=CC(=O)C2OC2C1=O)c1cccnc1O
Reaction #556887
7a
収率 72.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=CC(=O)C2OC2C1O)c1cccnc1O
Reaction #556888
compound 8a
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=CC(=O)C2OC2C1=O)c1cc2ccccc2nc1O
Reaction #556890
title product
収率 102.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)c1cnc(Cl)cc1NC(C)C)C(C)=O
Reaction #682590
ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(-c2cnc(Cl)cc2NC(C)C)oc1C
Reaction #682591
ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)c1cnc(Cl)cc1NC(C)C)C(C)=O
Reaction #682664
ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(-c2cnc(Cl)cc2NC(C)C)oc1C
Reaction #682665
ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2cncc(C(=O)NCC(=O)c3ccc(OC)cc3)c2)c(C)[nH]c1=O
Reaction #786276
DOI: 10.1039/C8SC04228D
COC(=O)Cc1nc(-c2ccc(Cl)nc2)oc1C
Reaction #941732
oxazole
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1nc(-c2ccc(Cl)nc2)oc1C
Reaction #947838
oxazole
収率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)c1cnc(Cl)cc1NC(C)C)C(C)=O
Reaction #964731
ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(-c2cnc(Cl)cc2NC(C)C)oc1C
Reaction #964732
ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(CN2CCOCC2)cc1
Reaction #1048256
DOI: 10.1039/C8SC04228D
CC(C)(C)C(O)CNC(=O)c1cccnc1SCCCc1ccc(F)cc1
Reaction #1235570
DOI: 10.1039/C8SC04228D
CO/N=C1\CCCC[C@@H]1NC(=O)c1cnc(OCC2CC2)c(-c2ccc(Cl)cc2)c1
Reaction #1271566
title compound
収率 36.4%DOI: 10.6084/m9.figshare.5104873.v1
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