5-Bromo-2-phenylpyrimidine → HCID 22099064, compound

HRID 1457490Notes

Reaction equation

HRID 1457490 reaction equation
[C:1]1([C:7]2[N:12]=[CH:11][C:10](Br)=[CH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:14]([O:24][C:25]1[CH:30]=[CH:29][C:28](B(O)O)=[CH:27][N:26]=1)=[CH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>>[CH2:14]([O:24][C:25]1[CH:30]=[CH:29][C:28]([C:10]2[CH:9]=[N:8][C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[N:12][CH:11]=2)=[CH:27][N:26]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH:22]=[CH2:23]

Participants

3

Reactant 2

HCID 143877455-Bromo-2-phenylpyrimidineHCID 57256129HCID 57256129, compound

Product 1

HCID 22099064HCID 22099064, compound

Procedure

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

Sources & evidence

ORD record
ord-9378181461ae4be8b2d0d51e258597ca
Source dataset
uspto-grants-1998_12
Patent number
US05849216

Reaction notes

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