Teilstruktursuche

4658

C#CCN(OC)C(=O)c1ccc(Cl)cc1
Reaction #3500
N-methoxy-N-propargyl-p-chlorobenzamide
Ausbeute 36.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOC(=NOC)c1ccc(Cl)cc1Cl
Reaction #3501
propargyl N-methoxy-2,4-dichlorobenzimidate
Ausbeute 29.8%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)c1ccc(Cl)c(Cl)c1
Reaction #51805
title compound
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CC1Oc2ccc(Cl)cc2C(=O)N1O
Reaction #56156
6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1, 3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CC1Oc2ccc(Cl)cc2C(=O)N1O
Reaction #56250
6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1,3-benzoxazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2ccc(Cl)cc2)c(C(=O)O)c1
Reaction #58264
2-(4-chlorobenzoyl)-5-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CONC(=O)c1ccc(Cl)cc1Nc1cc(Nc2cc(C)nn2C(C)C)ncc1Cl
Reaction #90810
4-Chloro-2-[(5-chloro-2-{[3-methyl-1-(1-methylethyl)-1H-pyrazol-5-yl]amino}-4-pyridinyl)amino]-N-(methyloxy)benzamide
Ausbeute 29.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(c2ccc(C(=O)c3ccc(Cl)c(S(N)(=O)=O)c3)cc2)C1
Reaction #224551
DOI: 10.1039/C8SC04228D
CC(C)COc1ccc(C(=O)c2ccc(Cl)c(S(N)(=O)=O)c2)cc1
Reaction #232178
DOI: 10.1039/C8SC04228D
COCN(c1cc(Cl)ccc1C=O)S(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #263999
DOI: 10.1039/C8SC04228D
N#Cc1cc2c3c(cccc3c1N1CCCC1)C(=O)N(OCc1ccccc1)C2=O
Reaction #280658
DOI: 10.1039/C8SC04228D
O=Cc1ccc(Cl)c(-n2cccc2)c1
Reaction #288610
DOI: 10.1039/C8SC04228D
CON(C)C(=O)c1ccc(Cl)cc1N
Reaction #289351
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1cc(C(=O)c2cccs2)ccc1Cl
Reaction #290605
DOI: 10.1039/C8SC04228D
COC(OC)c1cc(C(=O)c2ccc(Cl)cc2)c(Sc2ccc(Cl)cc2)s1
Reaction #299148
DOI: 10.1039/C8SC04228D
Cc1cccc(Cn2cc(C(=O)c3ccc(Cl)cc3)c(=O)c3ccccc32)n1
Reaction #314314
3-(4-chloro-benzoyl)-1-(6-methyl-pyridin-2-ylmethyl)-1H-quinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #363044
product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #363045
product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c3c(cccc3c1N1CCCC1)C(=O)N(OCc1ccccc1)C2=O
Reaction #366151
title compound
Ausbeute 68.6%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c3c(cccc3c1N1CCCCC1)C(=O)N(OCc1ccccc1)C2=O
Reaction #366152
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter