(6-Phenylpyridin-3-yl)boronic acid → HCID 22099047, compound

HRID 1457491Notes

Reaction equation

HRID 1457491 reaction equation
[CH:1]([O:11][C:12]1[N:17]=[CH:16][C:15](Br)=[CH:14][N:13]=1)=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[C:19]1([C:25]2[CH:30]=[CH:29][C:28](B(O)O)=[CH:27][N:26]=2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH2:1]([O:11][C:12]1[N:17]=[CH:16][C:15]([C:28]2[CH:29]=[CH:30][C:25]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[N:26][CH:27]=2)=[CH:14][N:13]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Participants

3

Reactant 2

HCID 2762710(6-Phenylpyridin-3-yl)boronic acidHCID 57140130HCID 57140130, compound

Product 1

HCID 22099047HCID 22099047, compound

Procedure

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

Sources & evidence

ORD record
ord-bfdf68cfee6e4245808b2f6b612feb38
Source dataset
uspto-grants-1998_12
Patent number
US05849216

Reaction notes

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