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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259393Generated: November 2, 2026

Methanol → 1-(2,3-Dihydroxy-propyl)-cyclopropanesulfonic acid [7-(2-fluoro-4-iodo-phenylamino)-6-methyl-5-oxo-2,3-dihydro-5H-oxazolo[3,2-a]pyridin-8-yl]-amide

https://huagongshe.com/reaction/1259393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Allyl-cyclopropanesulfonic acid [7-(2-fluoro-4-iodo-phenylamino)-6-methyl-5-oxo-2,3-dihydro-5H-oxazolo[3,2-a]pyridin-8-yl]-amideHCID 58380555—
CatalystOsmium TetroxideHCID 30318—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-(2,3-Dihydroxy-propyl)-cyclopropanesulfonic acid [7-(2-fluoro-4-iodo-phenylamino)-6-methyl-5-oxo-2,3-dihydro-5H-oxazolo[3,2-a]pyridin-8-yl]-amideHCID 5293409411%

Reaction Steps

Osmium tetra oxide (8 mg, 0.003 mmol), N-methyl morpholine (8 mg, 0.068 mmol) and water (0.5 mL) were added to a stirred solution of 1-allyl-cyclopropanesulfonic acid [7-(2-fluoro-4-iodo-phenylamino)-6-methyl-5-oxo-2,3-dihydro-5H-oxazolo[3,2-a]pyridin-8-yl]-amide (I-9a: 0.04 g, 0.073 mmol) in THF (5 mL). The resulting mixture was stirred at room temperature overnight. The reaction was monitored by TLC (5% MeOH in DCM). The reaction mixture was partitioned between ethylacetate and water. The organic layer was washed with water, brine solution, dried over Na2SO4 and concentrated. Purification by thin layer chromatography on silica gel (5% MeOH in DCM) afforded 0.005 g of the product (11% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466289B2
Source datasetuspto-grants-2013_06
ORD IDord-4fdc7575ae2a4f228a8fffb3fab8ee9a
Source noteuspto-grants-2013_06