Benzyl Bromide → Methyl 5-methoxypyridine-2-carboxylate

HRID 1678060Notes

Reaction equation

C(Br)C1C=CC=CC=1.[CH2:9]([O:16][C:17]1[CH:18]=[CH:19][C:20]([C:23]([O:25][CH3:26])=[O:24])=[N:21][CH:22]=1)C1C=CC=CC=1>>[CH3:9][O:16][C:17]1[CH:18]=[CH:19][C:20]([C:23]([O:25][CH3:26])=[O:24])=[N:21][CH:22]=1

Participants

Reactant 2

HCID 7498Benzyl Bromide

HCID 15574702Methyl 5-(benzyloxy)picolinate2×

Product 1

HCID 14282457Methyl 5-methoxypyridine-2-carboxylate

Procedure

The following compound was prepared using benzyl bromide according to the procedure above for compound 206: Methyl 5-benzyloxypyridine-2-carboxylate (compound 207)

Workup

customThe following compound was prepared

Sources & evidence

ORD record: ord-71e28a5fe031452aa2e5cdaac0a752f0
Source dataset: uspto-grants-2011_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08008487B2

Reaction notes

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