子结构搜索

7187

COc1cccc(NN)c1.Cl
Reaction #4479
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nn(-c2cccc(OC)c2)c1C
Reaction #8167
1-(3-methoxyphenyl)-3,5-dimethyl-1H-pyrazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]n(-c2cc(OC3CCCC3)c(Cl)cc2F)c2c1CCCC2
Reaction #49746
(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-1,2,4,5,6,7-hexahydro-3H-indazol-3-one
收率 72.3%DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49769
2-fluoro-4-chloro-5-cyclopentyloxyphenylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #56187
hydrogen chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(NN)c(Cl)cc1Cl
Reaction #63699
2,4-dichloro-5-(1-methylethoxy)phenylhydrazine
收率 68.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2cc(OC(C)C)c(Cl)cc2Cl)c(=O)[nH]c1=O
Reaction #63700
2-[2,4-dichloro-5-(1-methylethoxy)phenyl]-6-methyl-1,2,4-triazine-3,5(2H,4H)-dione
收率 58.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC(=O)C(C#N)=NNc1ccc(C(C#N)c2ccc(Cl)cc2)c(OC)c1
Reaction #63830
ethyl [2-[[4-[(4-chlorophenyl)cyanomethyl]-3-methoxyphenyl]hydrazono]-2-cyanoacetyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(C#N)c(=O)[nH]c2=O)ccc1C(C#N)c1ccc(Cl)cc1
Reaction #63831
2-[4-[(4-chlorophenyl)cyanomethyl]-3-methoxyphenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(NN=CC(=O)C(F)(F)F)c(F)cc1Cl
Reaction #76761
3,3,3-trifluoro-2-oxo-propanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(NN=CC(=O)C(F)(F)F)c(F)cc1Br
Reaction #76768
3,3,3-trifluoro-2-oxopropanal 1-(4-bromo-2-fluoro-5-isopropoxyphenylhydrazone)
收率 67.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2c(F)cccc2Cl)cc1OC
Reaction #87528
desired product
收率 89.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87529
desired product
收率 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2c(Cl)cccc2Cl)cc1OC
Reaction #87539
desired product
收率 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(Cl)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87540
desired product
收率 103.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)cc1OC
Reaction #87547
desired product
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87551
desired product
收率 46.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2cc(CNC(=O)C(F)(F)F)ccc2Cl)ccc1[N+](=O)[O-]
Reaction #87571
desired product
收率 74.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)ccc1[N+](=O)[O-]
Reaction #87572
desired product
收率 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c3c([nH]c2c1)CC(NC(C)=O)CC3
Reaction #95064
title compound
DOI: 10.6084/m9.figshare.5104873.v1
第 1 页下一页