4-pyridine-boronic acid

Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccncc3)c2c1
Reaction #7348
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-pyridinyl)quinolin-6-ol
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(-c2nc3ccccc3o2)ccc1Cc1ccncc1
Reaction #7848
2-[3-methoxy-4-(pyridin-4-ylmethyl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1[nH]c(=O)n(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1-c1ccncc1
Reaction #41048
title compound
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
Reaction #41907
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
Выход 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)N(Cc1cc(-c2ccncc2)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45350
Methyl{[5 ′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}[3-pyridin-4-yl-5-(trifluoromethyl)benzyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)Nc1ccc(-c2csc3c(-c4ccncc4)cnc(N)c23)cc1
Reaction #45409
desired product
Выход 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccncc3)c2c1
Reaction #53692
2-methylsulfonyl-N-(3-pyridin-4-yl-1H-indazol-5-yl)benzenesulfonamide
Выход 15.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1c(C(=O)OC(C)(C)C)oc2cccc(-c3ccncc3)c12
Reaction #57645
3-methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid tert-butyl ester
Выход 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1c(-c2ccncc2)nc(-c2ccccc2)c1-c1nc2c(N)ncnc2s1
Reaction #60830
title compound
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1NCCc2c(-c3ccncc3)[nH]c3cccc1c23
Reaction #61602
2-pyridin-4-yl-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1cc(-c2ccncc2)c2[nH]c3c(c2c1)CN1CCC3CC1
Reaction #66091
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
Reaction #67383
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
Выход 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N(Cc1ccc2c(c1)OCCO2)C1CCN(CCn2c(=O)cc(-c3ccncc3)c3ccccc32)CC1
Reaction #68224
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(2-oxo-4-(pyridin-4-yl)quinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(-c3ccncc3)cc2n1Cc1ccccc1
Reaction #68417
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(-c3ccncc3)cc2n1Cc1ccccn1
Reaction #68420
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC[C@@H]1C(=O)N(C)c2cnc(-c3cccnc3-c3ccccc3)nc2N1c1ccn(C)n1
Reaction #73176
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(C)ccc1-c1ccncc1
Reaction #88848
title compound
Выход 48.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(c1c(-c2ccncc2)ccc2c1OCO2)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88859
title compound
Выход 170.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(F)cc1-c1ccncc1
Reaction #88866
title compound
Выход 59.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cccnc1-c1ccncc1
Reaction #88871
title compound
Выход 70.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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