Methyl iodide → HCID 9806308, compound

HRID 257148Notes

Reaction equation

HRID 257148 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:17]=[C:18]([C:20]2([O:26][CH3:27])[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)[CH:19]=1)[O:5][CH2:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[N:13]=[CH:12][CH:11]=[CH:10]2.[CH3:28][I:29]>C(#N)C>[I-:29].[F:1][C:2]1[CH:3]=[C:4]([CH:17]=[C:18]([C:20]2([O:26][CH3:27])[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)[CH:19]=1)[O:5][CH2:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[N+:13]([CH3:28])=[CH:12][CH:11]=[CH:10]2

Participants

4

Reactant 2

HCID 6328Methyl iodideHCID 10904659HCID 10904659, compound

Product 1

HCID 9806308HCID 9806308, compoundYield 57%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A mixture of 6-[(3-fluoro-5-[4-methoxy-3,4,5,6-tetrahydro-2H-pyran -4-yl]phenoxy)methyl]quinoline (0.367 g), methyl iodide (0.2 ml) and acetonitrile (7 ml) was stirred at ambient temperature for 16 hours. The precipitate was filtered off to give 6-[(3-fluoro-5-[4-methoxy -3,4,5,6-tetrahydro-2H-pyran-4-yl]phenoxy)methyl]-1-methylquinolinium iodide (0.29 g) in 57% yield, m.p. 190° C.

Workup

  1. filtrationThe precipitate was filtered off

Sources & evidence

ORD record
ord-68fe5073d43e429eb7b9c06c88b174c7
Source dataset
uspto-grants-1993_11
Patent number
US05260442

Reaction notes

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