2-Methoxyethanol → HCID 21109684, compound

HRID 1766494Notes

Reaction equation

HRID 1766494 reaction equation
CO[C:3](=[O:12])[C:4]1[CH:9]=[C:8](Br)[C:7]([OH:11])=[N:6][CH:5]=1.[Cl:13][C:14]1[CH:19]=[CH:18][C:17](B(O)O)=[CH:16][CH:15]=1.[NH2:23][CH2:24][CH:25]([CH2:28][CH2:29][CH3:30])[CH2:26][OH:27].[CH3:31][O:32][CH2:33][CH2:34]O>>[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([C:8]2[C:7]([O:11][CH2:34][CH2:33][O:32][CH3:31])=[N:6][CH:5]=[C:4]([CH:9]=2)[C:3]([NH:23][CH2:24][CH:25]([CH2:26][OH:27])[CH2:28][CH2:29][CH3:30])=[O:12])=[CH:16][CH:15]=1

Participants

5

Reactant 4

HCID 80192-MethoxyethanolHCID 742994-Chlorophenylboronic acidHCID 2764315Methyl 5-bromo-6-hydroxynicotinateHCID 21109696HCID 21109696, compound

Product 1

HCID 21109684HCID 21109684, compound

Procedure

The title compound was synthesized in analogy to Example 102, using 5-bromo-6-hydroxy-nicotinic acid methyl ester, 2-methoxyethanol, (4-chloro-phenyl)-boronic acid and 2-(aminomethyl)-1-pentanol as starting materials to yield (RS)-5-(4-chloro-phenyl)-N-(2-hydroxymethyl-pentyl)-6-(2-methoxy-ethoxy)-nicotinamide. MS (ISP) 407.5 (M+H)+.

Workup

  1. customThe title compound was synthesized in analogy to Example 102

Sources & evidence

ORD record
ord-832df8b7fb604bf7b19bcccb5d1d70cc
Source dataset
uspto-grants-2007_06
Patent number
US07229999B2

Reaction notes

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