Pyrimidine, 2-methoxy- → HCID 20029028, compound

HRID 1722578Notes

Reaction equation

HRID 1722578 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][CH:6]=[CH:5][N:4]=1.[F:9][B-:10]([F:13])([F:12])[F:11].[CH3:14][O+](C)C>C(Cl)Cl>[F:9][B-:10]([F:13])([F:12])[F:11].[CH3:14][N+:4]1[CH:5]=[CH:6][CH:7]=[N:8][C:3]=1[O:2][CH3:1]

Participants

4

Reactant 2

HCID 136730Pyrimidine, 2-methoxy-HCID 2735153Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)

Product 1

HCID 20029028HCID 20029028, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Starting material prepared by reaction of 2-methoxypyrimidine with trimethyloxonium tetrafluoroborate in CH2Cl2 at ambient temperature for 4 hours to give 1-methyl-2-methoxypyrimidinium tetrafluoroborate.

Sources & evidence

ORD record
ord-69b50c7077fc46fab02550ebf63fb1f1
Source dataset
uspto-grants-1989_08
Patent number
US04855420

Reaction notes

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