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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552739Generated: October 29, 2026

2,6-Di-tert-butyl-4-methylpyridine → HCID 86607324, compound

https://huagongshe.com/reaction/552739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylpyridineHCID 98898—
Reactanttert-butyl N-(chlorosulfonyl)carbamateHCID 15677406—
ReactantHCID 67164234HCID 67164234—
Solvent2-OxopropiononitrileHCID 69430—
ProductHCID 86607324HCID 8660732441.4%

Reaction Steps

To a solution of (2R,3S,5R)-5-(5-ethyl-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol (0.0560 g, 0.213 mmol) and 2,6-di-tert-butyl-4-methylpyridine in AcCN (4 mL) at 0° C. was added tert-butyl(chlorosulfonyl)carbamate (0.0573 g, 0.266 mmol), the solution was warmed to room temperature and stirred for 1 hour. The reaction was quenched with 7N ammonia in methanol (2 mL) and concentrated. The residue was purified by flash chromatography (0 to 10% MeOH/DCM) to give the title compound as a white solid (39 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951810B2
Source datasetuspto-grants-2011_05
ORD IDord-be624c2ddfdf448a8b1e00a3abc836c5
Source noteuspto-grants-2011_05