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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241042Generated: November 1, 2026

Potassium Carbonate → (R)-1-(2-amino-5-bromopyridin-3-ylsulfonyl)pyrrolidin-3-ol

https://huagongshe.com/reaction/241042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-3-PyrrolidinolHCID 2759337—
Reactant2-Amino-5-bromopyridine-3-sulfonyl chlorideHCID 53302026—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(R)-1-(2-amino-5-bromopyridin-3-ylsulfonyl)pyrrolidin-3-olHCID 6682021273%

Reaction Steps

To a solution of (R)-pyrrolidin-3-ol (32 mg, 0.37 mmol) and potassium carbonate (102 mg, 0.74 mmol) in dioxane (2 mL) and water (400 uL) was added 2-amino-5-bromopyridine-3-sulfonyl chloride (100 mg, 0.37 mmol, prepared according to the methods in WO2008144463). The reaction mixture was stirred for 2 h at rt. Saturated sodium bicarbonate was then added, and the aqueous solution was extracted twice with ethyl acetate. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo to provide (R)-1-(2-amino-5-bromopyridin-3-ylsulfonyl)pyrrolidin-3-ol (87.3 mg, 0.27 mmol, 73% yield) as a white solid. 1H NMR (400 MHz, DMSO-D6-d6) δ 8.31 (d, 1H), 7.92 (d, 1H), 6.85 (br s, 2H), 5.02 (br s, 1H), 4.23 (dt, 1H), 3.38-3.25 (m, 3H), 3.14-3.06 (m, 1H), 1.92-1.81 (m, 1H), 1.77-1.67 (m, 1H); MS (EI) for C9H12BrN3O3S: 322, 324 (Br isotopes, MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-bb968e8e42c54d8f902e16e53f228084
Source noteuspto-grants-2014_02