(Pyridin-4-yl)boronic acid → HCID 59553194, compound

HRID 1171387Notes

Reaction equation

HRID 1171387 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:27]=[CH:28][CH:29]=1)[C:5]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]([O:18][CH2:19][CH2:20][N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)=[CH:10][CH:9]=1)=[O:6].B(O)(O)[C:31]1[CH:36]=[CH:35][N:34]=[CH:33][CH:32]=1>>[N:21]1([CH2:20][CH2:19][O:18][C:11]2[C:12]3[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=3)[C:8]([NH:7][C:5](=[O:6])[C:4]3[CH:27]=[CH:28][CH:29]=[C:2]([C:31]4[CH:36]=[CH:35][N:34]=[CH:33][CH:32]=4)[CH:3]=3)=[CH:9][CH:10]=2)[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1

Participants

3

Reactant 2

HCID 2734379(Pyridin-4-yl)boronic acidHCID 595531183-bromo-N-[4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl]-benzamide

Product 1

HCID 59553194HCID 59553194, compound

Procedure

Compound is prepared from 3-bromo-N-[4-(2-morpholin-4-yl-ethoxy)-naphthalen-1-yl]-benzamide and pyridyl-4-boronic acid according to conditions described in general procedure K. 1H NMR 300 MHz (DMSO-d6) δ 10.4 (s, 1H), 8.7 (d, 2H), 8.5 (s, 1H), 8.22 (m, 1H), 8.15 (d, 1H), 8.05 (d, 1H), 7.9 (m, 1H), 7.85 (d, 2H), 7.7 (t, 1H), 7.5 (m, 2H), 7.45 (d, 1H), 7.0 (d, 1H), 4.3 (t, 2H), 3.6 (m, 4H), 2.9 (t, 2H), 2.55 (m, 4H).

Sources & evidence

ORD record
ord-cdf5cd5f00cd439c8a87f71fe3e557ab
Source dataset
uspto-grants-2010_11
Patent number
US07829560B2

Reaction notes

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