4-Cyanophenylboronic acid → HCID 18448303, compound

Reaction equation

Br[C:2]1[C:3]([CH3:28])=[C:4]([N:8]([CH2:13][C:14]2[CH:26]=[CH:25][C:17]([O:18][CH2:19][C:20]([O:22]CC)=[O:21])=[C:16]([CH3:27])[CH:15]=2)[CH2:9][CH2:10][CH2:11][CH3:12])[CH:5]=[CH:6][CH:7]=1.[C:29]([C:31]1[CH:36]=[CH:35][C:34](B(O)O)=[CH:33][CH:32]=1)#[N:30]>>[CH2:9]([N:8]([CH2:13][C:14]1[CH:26]=[CH:25][C:17]([O:18][CH2:19][C:20]([OH:22])=[O:21])=[C:16]([CH3:27])[CH:15]=1)[C:4]1[C:3]([CH3:28])=[C:2]([C:34]2[CH:35]=[CH:36][C:31]([C:29]#[N:30])=[CH:32][CH:33]=2)[CH:7]=[CH:6][CH:5]=1)[CH2:10][CH2:11][CH3:12]

Participants

Reactant 2

HCID 27343264-Cyanophenylboronic acid

HCID 58622888HCID 58622888, compound

Product 1

HCID 18448303HCID 18448303, compound

Procedure

Prepared from ethyl (4-{[(3-bromo-2-methylphenyl)(butyl)amino]methyl}-2-methylphenoxy)acetate and 4-cyanophenylboronic acid using the procedure described for Example 25 (Method A).

Sources & evidence

ORD record: ord-9aab9032a94842e9bc9294cde916432d
Source dataset: uspto-grants-2007_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07199239B2

Reaction notes

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