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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241601Generated: October 30, 2026

Triethylamine → 2-(5-Bromopyridin-3-yl)-2-azabicyclo[3.1.0]hex-3-ylmethyl methanesulfonate

https://huagongshe.com/reaction/241601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67297729HCID 67297729—
SolventDichloromethaneHCID 6344—
Product2-(5-Bromopyridin-3-yl)-2-azabicyclo[3.1.0]hex-3-ylmethyl methanesulfonateHCID 8667491490%

Reaction Steps

To an ice-cold solution of [2-(5-Bromopyridin-3-yl)-2-azabicyclo[3.1.0]hex-3-yl]methanol (462 mg, 2.43 mmol) in dry dichloromethane (10 mL) was added triethylamine (0.51 mL, 3.6 mmol) followed by methanesulfonyl chloride (334 mg, 2.92 mmol). The reaction mixture was gradually warmed to room temperature and stirred for 1 hour. The volatiles were removed under reduced pressure and the crude product was purified by flash column chromatography to obtain title compound of 586 mg as gummy liquid. Yield: 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653071B2
Source datasetuspto-grants-2014_02
ORD IDord-3ba3678bc5f94c3eba5e6deaa328a185
Source noteuspto-grants-2014_02