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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217618Generated: October 29, 2026

Triacetoxyperiodinane → isobutane-1-sulfonic acid [3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]-amide

https://huagongshe.com/reaction/217618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant2-methyl-propane-1-sulfonic acid {3-[(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)-hydroxy-methyl]-2,4-difluoro-phenyl}-amideHCID 59569597—
SolventTetrahydrofuranHCID 8028—
Productisobutane-1-sulfonic acid [3-(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]-amideHCID 5956961941.9%

Reaction Steps

In a round bottom flask, 2-methyl-propane-1-sulfonic acid {3-[(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)-hydroxy-methyl]-2,4-difluoro-phenyl}-amide (68, 618 mg, 1.30 mmol) was dissolved in 20 mL of tetrahydrofuran, and Dess-Martin periodinane (555 mg, 1.31 mmol) was added. The reaction was stirred at room temperature for 30 minutes, then quenched with water and extracted with ethyl acetate. The organic layer was washed with sodium bicarbonate, water, and brine, then dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with dichloromethane and methanol. Appropriate fractions were collected and concentrated under vacuum to provide the desired compound (69, 257 mg). MS (ESI) [M−H+]−=469.9, 471.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198273B2
Source datasetuspto-grants-2012_06
ORD IDord-b6f942ea4404409891e5b78b28c9dece
Source noteuspto-grants-2012_06