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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366079Generated: October 27, 2026

tert-Butanol → 6-chloro-N-cyclopentyl-N-(2,3-dihydroxypropyl)pyridine-3-sulfonamide

https://huagongshe.com/reaction/2366079

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantMethyl morpholine oxideHCID 82029—
Reactant6-chloro-N-cyclopentyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamideHCID 61045603—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Product6-chloro-N-cyclopentyl-N-(2,3-dihydroxypropyl)pyridine-3-sulfonamideHCID 8665995875%

Reaction Steps

To a solution of 1.1 g (3.7 mmol) of 6-chloro-N-cyclopentyl-N-(prop-2-en-1-yl)pyridine-3-sulfonamide in 15 mL of a mixture (1/1) of tBuOH and water are added, at room temperature, 1.2 g (10.3 mmol) of NMO and 0.52 mL (0.04 mmol) of 2.5% OsO4 in tBuOH. Stirring is continued for 12 hours. The medium is then diluted with 200 mL of water and extracted with Et2O (2×100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. 0.92 g of 6-chloro-N-cyclopentyl-N-(2,3-dihydroxypropyl)pyridine-3-sulfonamide is obtained in the form of a brown solid, which is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697731B2
Source datasetuspto-grants-2014_04
ORD IDord-e4ae56011fc144638b5432536c5443a1
Source noteuspto-grants-2014_04