مشارك في 176 تفاعل

1126167

c1ncc2cn[nH]c2n1
Reaction #53248
pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CS(=O)(=O)CC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60298
crude desired product
المردود 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1cc(F)nc2ccccc12
Reaction #75705
2-fluoroquinoline-4-carboxylic acid methyl ester
المردود 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)C(=Cc1ccc(C#N)cc1OC[C@@H](CCC(=O)OCc1ccccc1)NC(=O)c1cccc(-c2ccc(NC(=N)N)cc2)c1)NC(C)=O.O=C(O)C(F)(F)F
Reaction #78214
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOc1cc(C(N)=CS(C)(=O)=O)ccc1OC
Reaction #84210
product
المردود 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN(C)c1cc(C(=O)CS(C)(=O)=O)cc(N(C)C)c1
Reaction #209593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCc1ccccc1
Reaction #216555
methyl 3-phenylpropionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CS(=O)(=O)CCc1cccc(I)c1
Reaction #229871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)CC(=O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #242202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)CC(O)c1ccc(-c2ccc(C(CC3CCOCC3)c3ccc(S(=O)(=O)C4CC4)cc3)[nH]2)nc1
Reaction #254978
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(=O)c1ccnc(S(C)(=O)=O)c1
Reaction #284685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NC(CS(C)(=O)=O)c1ccccc1Cl
Reaction #287550
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CS(=O)(=O)CC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #303663
crude desired product
المردود 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CS(=O)(=O)CC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #303752
crude desired product
المردود 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CS(=O)(=O)CC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #304239
crude desired product
المردود 97.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)NC(CS(C)(=O)=O)c1ccccc1Cl
Reaction #307843
title compound
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)NC(CS(C)(=O)=O)c1cccc(C(F)(F)F)c1
Reaction #307844
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CS(=O)(=O)CC(=O)c1ccccc1N
Reaction #368427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CS(=O)(=O)C=C(N)C1(c2ccc(Cl)cc2)CCC1
Reaction #380818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOc1cc(C(N)CS(C)(=O)=O)ccc1OC
Reaction #391466
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
الصفحة 1التالي