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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948537Generated: October 31, 2026

Hydroxyamine hydrochloride → HCID 58374179, compound

https://huagongshe.com/reaction/1948537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant(S)-ethyl 1-(1-(4-cyanophenyl)-2-methyl-1-oxopropan-2-yl)piperidine-3-carboxylateHCID 68260699—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 58374179HCID 58374179100.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of (S)-ethyl 1-(1-(4-cyanophenyl)-2-methyl-1-oxopropan-2-yl)piperidine-3-carboxylate (90 mg, 0.274 mmol) in MeOH (5 mL) was added sodium borohydride (15 mg, 0.396 mmol). After 1 hr, the reaction was quenched with water. The reaction mixture was diluted with ethyl acetate and washed with sat NaCl. The organic layer was dried MgSO4, filtered, and concentrated. To a mixture of hydroxylamine hydrochloride (38.1 mg, 0.548 mmol) and sodium bicarbonate (92 mg, 1.096 mmol) in 2-propanol (10 mL) was added the crude product from step one. The reaction mixture was heated at 75° C. overnight. The reaction mixture was diluted with ethyl acetate and washed with H2O. The organic layer was dried MgSO4, filtered, and concentrated to yield 100 mg of (3S)-ethyl 1-(1-hydroxy-1-(4-((Z)—N′-hydroxycarbamimidoyl)phenyl)-2-methylpropan-2-yl)piperidine-3-carboxylate. MS (m+1)=364. HPLC Peak RT=0.27 minutes (Analytical Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399451B2
Source datasetuspto-grants-2013_03
ORD IDord-dff7b0df98154f23a8fde924ce0afc0b
Source noteuspto-grants-2013_03