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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627660Generated: November 1, 2026

Dimethylformamide → HCID 86728127, compound

https://huagongshe.com/reaction/627660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant2-(Methylsulfonyl)ethanolHCID 84834—
ReactantHCID 86728128HCID 86728128—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 86728127HCID 8672812794.4%

Reaction Steps

To a solution of (R)-tert-butyl-N-(5-(2-fluoro-5-nitrophenyl)-2,2,5-trimethyl-1,1-dioxido-5,6-dihydro-2H-1,4-thiazin-3-yl)-N-tert-butoxycarbonyl-carbamate (1.00 g, 1.888 mmol) (prepared according to the procedure detailed in Intermediate 32, Step 1) in DMF (8 ml) 2-(methylsulphonyl)ethanol (0.49 g, 3.95 mmol) and cesium carbonate (1.28 g, 3.93 mmol) were added and the mixture was stirred overnight at rt. Additional Cs2CO3 (610 mg, 1 eq) and 2-(methylsulphonyl)ethanol (250 mg, 1 eq) were added and stirring continued for additional 2 hrs. The mixture was diluted with EtOAc and saturated ammonium chloride. Organic layer was separated and washed twice with water, then with brine and concentrated. The residue was purified by FC on 40 g RediSep Gold column using 5-100% EtOAc in heptane to afford (R)-tert-butyl-N-(5-(2-hydroxy-5-nitrophenyl)-2,2,5-trimethyl-1,1-dioxido-5,6-dihydro-2H-1,4-thiazin-3-yl)-N-tert-butoxylcarbonyl-carbamate (940 mg, 1.782 mmol, 94% yield). LC/MS (ESI+) m/z=550 (M+Na)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-d6902cc8ef9a48c1955fb9e52921dce4
Source noteuspto-grants-2016_04