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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102411Generated: November 1, 2026

O-ethylhydroxylamine hydrochloride → HCID 11326327, compound

https://huagongshe.com/reaction/2102411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 69009937HCID 69009937—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11326327HCID 11326327—

Reaction Conditions

Temperature0 °C

Reaction Steps

O-Ethyl-hydroxylamine HCl salt (2.50 equivalents) is added to a solution of 6-(2-fluoro-4-methylsulfanyl-phenylamino)-7-methylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid ethyl ester (1.00 equivalent) in THF. The solution is cooled to 0° C. and lithium bis(trimethylsilyl)amide (6.00 equivalents, 1.0 M solution in hexanes) is added dropwise. The reaction mixture is warmed to room temperature. After stirring for 1 hour, the reaction is quenched by addition of a saturated aqueous solution of NaHCO3 and partitioned between EtOAc and brine. The aqueous layer is re-extracted with EtOAc. The combined organic extracts is dried (MgSO4) and concentrated. The product is purified by flash chromatography as necessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576072B2
Source datasetuspto-grants-2009_08
ORD IDord-29d90103cc844203bbd9231153509db3
Source noteuspto-grants-2009_08