HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102411Generated: November 1, 2026
O-ethylhydroxylamine hydrochloride → HCID 11326327, compound
https://huagongshe.com/reaction/2102411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 69009937 | HCID 69009937 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11326327 | HCID 11326327 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576072B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-29d90103cc844203bbd9231153509db3 |
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| Source note | uspto-grants-2009_08 |
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