Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211683Generated: October 31, 2026

Sodium Sulfite → HCID 10309658, compound

https://huagongshe.com/reaction/2211683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantMethanesulfonamideHCID 72879—
ReactantHCID 18684838HCID 18684838—
Solvent2-Methylpropan-2-ol--water (1/1)HCID 71401949—
ProductHCID 10309658HCID 10309658—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (S)-N-[[3-[4-(3,6-dihydro-1,1-dioxido-2H-thiopyran-4-yl)-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (0.415 g, 1.08 mmol; prepared as described in U.S. Pat. No. 5,968,962) in 1:1 t-butanol-water (4 mL) is added to a solution of the standard reagent AD mix-β (1.51 g; available from Aldrich Co.) and methanesulfonamide (0.103 g, 1.08 mmol) in 1:1 t-butanol-water (10 mL) cooled at 0° C. The reaction mixture is stirred 5 days at 4° C. and then treated with sodium sulfite (1.5 g) and stirred 30 minutes. The solution is then extracted with four 10 mL portions of ethyl acetate and the combined organic phases dried (MgSO4), filtered and concentrated. Purification by column chromatography (0–5% MeOH-DCM) provided the title compound as a mixture of diastereomers. Yield 0.29 g (64%). 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101874B2
Source datasetuspto-grants-2006_09
ORD IDord-74ae24fce0a444e49c338316288f02c8
Source noteuspto-grants-2006_09