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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445737Generated: October 27, 2026

5-Bromo-3-isopropoxy-2-methylpyridine → 5-Bromo-3-isopropoxy-2-methyl-pyridine 1-oxide

https://huagongshe.com/reaction/445737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-3-isopropoxy-2-methylpyridineHCID 59612972—
Reactant(5-Bromo-2-methyl-pyridin-3-yl)-ethyl-carbamic acid tert-butyl esterHCID 59613068—
Product5-Bromo-3-isopropoxy-2-methyl-pyridine 1-oxideHCID 67266224—

Reaction Steps

The title compound was synthesized in a similar manner as described for Stage 155.1.4 using 5-bromo-3-isopropoxy-2-methyl-pyridine (Stage 84.1.2, 2.108 mmol) as replacement for (5-bromo-2-methyl-pyridin-3-yl)-ethyl-carbamic acid tert-butyl ester to give the title compound as a slowly crystallizing orange solid. (HPLC: tR 2.75 min (Method A); M+H=246, 248 MS-ES).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476294B2
Source datasetuspto-grants-2013_07
ORD IDord-925ed66be88e4cc7afb58a998ad8759b
Source noteuspto-grants-2013_07