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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036792Generated: November 1, 2026

2-Methoxyethylamine → HCID 61695057, compound

https://huagongshe.com/reaction/2036792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactant5-Bromopyridine-3-sulfonyl chlorideHCID 20324474—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61695057HCID 6169505727%

Reaction Steps

A solution of 5-bromopyridine-3-sulfonyl chloride (1.5 g, 5.8 mmol)) and 2-methoxyethanamine (1.3 g, 18 mmol) in THF (40 mL) was stirred at room temperature for 16 h. After this time, the resulting reaction mixture was partitioned between saturated aqueous sodium chloride and ethyl acetate. The organic solution was dried and evaporated. The resulting residue was purified by flash column chromatography using ethyl acetate/hexanes to yield 5-bromo-N-(2-methoxyethyl)pyridine-3-sulfonamide (460 mg, 27%). LCMS Method T: Retention time 1.13 min; [M+1]=295, 297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-51353fcce4134c6983c945bd7b3be1bc
Source noteuspto-grants-2013_11