21 件の反応に参加

247993

COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NC(=S)Nc1cc(Cl)cc(Cl)c1
Reaction #53770
1-(3,5-Dichloro-phenyl)-3-[5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-thiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NC(=S)Nc1ccc(C(=O)O)cc1
Reaction #53771
4-{3-[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-thioureido}-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NC(=S)Nc1cccc(C(=O)O)c1
Reaction #53772
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NS(=O)(=O)c1cc(Cl)cc(Cl)c1
Reaction #53773
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NS(=O)(=O)c1cccs1
Reaction #53774
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1cccs1
Reaction #53779
product
収率 32.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(CNc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1
Reaction #53780
product
収率 46.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1ccc(CNc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1
Reaction #53781
product
収率 26.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NS(=O)(=O)c1cccc([N+](=O)[O-])c1
Reaction #53782
N-[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-3-nitro-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCCCCCCCCS(=O)(=O)Nc1cc(-c2cc3cc(F)c(F)cc3[nH]2)ccc1OC
Reaction #53786
product
収率 44.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOP(=O)(Cc1ccc(NC(=S)Nc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1)OCC
Reaction #53792
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1N=C=S
Reaction #53797
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NC(=S)Nc1cccnc1
Reaction #53800
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1cccc([N+](=O)[O-])c1
Reaction #53805
product
収率 26.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
Reaction #53806
product
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])c(O)c1
Reaction #53807
product
収率 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc(O)c([N+](=O)[O-])c1
Reaction #53808
product
収率 35.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc(C#N)cc1
Reaction #53809
product
収率 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1cccc(C#N)c1
Reaction #53810
product
収率 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc([N+](=O)[O-])cc1
Reaction #184049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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