(6-Phenylpyridin-3-yl)boronic acid → HCID 22099057, compound

HRID 1457492Notes

Reaction equation

HRID 1457492 reaction equation
Br[C:2]1[N:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:4][N:3]=1.[C:20]1([C:26]2[CH:31]=[CH:30][C:29](B(O)O)=[CH:28][N:27]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:8]([C:5]1[CH:4]=[N:3][C:2]([C:29]2[CH:30]=[CH:31][C:26]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[N:27][CH:28]=2)=[N:7][CH:6]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]

Participants

3

Reactant 2

HCID 2762710(6-Phenylpyridin-3-yl)boronic acidHCID 22099059Pyrimidine, 2-bromo-5-dodecyl-

Product 1

HCID 22099057HCID 22099057, compound

Procedure

The synthesis was carried out analogously to Example 27 from 2-bromo-5-dodecylpyrimidine and 2-phenylpyridine-5-boronic acid.

Sources & evidence

ORD record
ord-2c10d110fcbe4b93872dbaaed129046d
Source dataset
uspto-grants-1998_12
Patent number
US05849216

Reaction notes

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