o-Anisidine

COc1ccccc1NS(=O)(=O)c1cccnc1
Reaction #2502
title compound
المردود 83.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(C)cc1
Reaction #2503
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(S(=O)(=O)Nc2ccccc2OC)cc1
Reaction #2504
title compound
المردود 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(F)cc1
Reaction #2505
title compound
المردود 93.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1cccc([N+](=O)[O-])c1
Reaction #2506
title compound
المردود 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(C(=O)O)cc1
Reaction #2510
title compound
المردود 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C(=O)Nc2ccccc2OC)c1
Reaction #2511
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc(C#N)cc1
Reaction #2512
title compound
المردود 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccncc1
Reaction #2513
title compound
المردود 97.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc(CCl)cc1
Reaction #2514
title compound
المردود 94.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #2517
title compound
المردود 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1cccc(CO)c1
Reaction #2545
title compound
المردود 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CC1OCCO1)C(=O)c1ccc(CCl)cc1
Reaction #2552
title compound
المردود 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NCCN1CCC(C(=O)c2ccc(F)cc2)CC1
Reaction #2557
title compound
المردود 66.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(C)c2n1
Reaction #3298
6-(2,6-Dichlorophenyl)-2-(2-methoxyphenylamino)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1ccccc1SSc1ccccc1C(=O)Nc1ccccc1OC
Reaction #3817
title compound
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(N)=S
Reaction #49959
N-(o-methoxyphenyl)thiourea
المردود 57.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccccc1N/C(=C1\C(=O)Nc2ccccc21)c1ccccc1
Reaction #53009
(Z)-3-[1-(2-methoxy-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccccc1NCC1OC(C)C(C)O1
Reaction #56312
N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCC1COC(CNc2ccccc2OC)O1
Reaction #56315
N-(4-ethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
الصفحة 1التالي