ethanol tetrahydrofuran

CC(=O)Nc1cc(N)c(Cl)cc1F
Reaction #1575
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(O)cc2)cc1
Reaction #2380
4-tert-butyl-N-{6-[2-(4-hydroxyphenoxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
المردود 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(N)cc2)cc1
Reaction #2381
N-{6-[2-(4-aminophenoxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide
المردود 98.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCCCN1CCNCC1)Nc1nc2ccc(Br)cc2s1
Reaction #9258
N-(6-Bromo-1,3-benzothiazol-2-yl)-N′-(3-piperazinopropyl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)CCCNC(=O)Nc1nc2ccc(Br)cc2s1
Reaction #9259
pure product
المردود 15.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCOc1ccc(N)cc1-c1nn2c(C3CCCC3)nc(C)c2c(=O)[nH]1
Reaction #11363
2-(5-Amino-2-propoxyphenyl)-5-methyl-7-cyclopentyl-3H-imidazo[5,1-f][1,2,4]-triazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CSc1ccc(Nc2cc(=O)n(C)nc2C(=O)NOCCO)c(F)c1
Reaction #44239
desired product
المردود 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Oc2cccc3occc23)c(F)c1
Reaction #44688
4-(1-Benzofuran-4-yloxy)-3-fluorophenylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Oc2cccc3[nH]ncc23)c(F)c1
Reaction #44691
3-Fluoro-4-(1H-indazol-4-yloxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCOCOc1cc(N)ccc1C#N
Reaction #46737
4-Amino-2-(2-methoxy-ethoxymethoxy)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)[Si](OC[C@H](C)Oc1cc(O)cc(C(=O)Nc2ccn(C(=O)OC(C)(C)C)n2)c1)(C(C)C)C(C)C
Reaction #48864
crude solid
المردود 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=NOCCCOc1ccc(CC(=O)O)cc1)c1ccc(C(C)(C)C)cc1
Reaction #57918
title compound
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60191
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(C#N)cc1
Reaction #60192
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(CCCO)[N+](=O)[O-]
Reaction #61662
4-methyl-4-nitro-pentan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)NC1=Nc2cc(-c3ccc(C(=O)N4CCCC4)cc3)ccc2C=C(C(=O)O)C1
Reaction #66263
(1E,4E)-2-(tert-butoxycarbonylamino)-8-(4-(pyrrolidine-1-carbonyl)phenyl)-3H-benzo[b]azepine-4-carboxylic acid
المردود 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)Nc1cc(N)c(Cl)cc1F
Reaction #80702
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(O)c1ccc(OCCCCl)c(O)c1
Reaction #83879
4-(3-chloropropoxy)-3-hydroxy-α-methylbenzene methanol
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #87330
raw product
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(S(=O)(=O)n2ncc3c2CCCC3O)cc1
Reaction #90726
1-tosyl-4,5,6,7-tetrahydro-1H-indazol-4-ol
المردود 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
الصفحة 1التالي