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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735993Generated: October 30, 2026

Sodium hydride → HCID 19434070, compound

https://huagongshe.com/reaction/1735993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-bromo-3-ethoxypropaneHCID 260493—
Reactant4-Hydroxy-3,4-dihydro-1lambda~6~-thieno[3,2-e][1,2]thiazine-1,1(2H)-dioneHCID 22901942—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 19434070HCID 1943407071%

Reaction Steps

A solution of the product from Example 1, Step C (13.0 g, 63.3 mmol) in DMF (50 mL) was added to a suspension of sodium hydride (2.5 g of a 60% slurry in mineral oil, washed with hexane, 63.3 mmol) in DMF (300 mL) at 0° C. After stirring for 45 min, the product from Step A (10.6 g, 63.3 mmol) was added and the mixture was stirred for 18 hr, during this time the temperature slowly increased to room temperature. The reaction mixture was diluted with cold water (300 mL) and extracted with ethyl acetate (5×10 mL). The combined extracts were washed with water (3×10 mL), saturated aqueous sodium chloride (20 mL), dried (MgSO4) and evaporated to a residue which was purified by column chromatography (silica, gradient, 3:1 hexane/ethyl acetate to 7:3 methylene chloride/methanol) to provide a clear oil (13.1 g, 71%) which was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538966
Source datasetuspto-grants-1996_07
ORD IDord-13c3309ba14e437bb6c9c1656ea435df
Source noteuspto-grants-1996_07