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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891017Generated: October 30, 2026

Hydroxylamine → HCID 3013463, compound

https://huagongshe.com/reaction/891017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
Reactantp-Xylyl bromideHCID 7721—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantEthyl Beta-Carboline-3-CarboxylateHCID 105078—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 3013463HCID 3013463—

Reaction Steps

To a stirred solution of ethyl 9H-β-carboline-3-carboxylate (400 mg, 1.67 mmol) in DMF (5 mL) under a nitrogen atmosphere was added NaH (73 mg, 60% in mineral oil, 1.76 mmol) portionwise, followed by 4-methylbenzyl bromide (308 mg, 1.67 mmol). Stirring was continued for 48 hours at ambient temperature, water (50 mL) was then added to the mixture. The precipitate was filtered, washed with water and dried to give a solid that was dissolved in methanol (35 mL). To the resulting solution, NaOH (2N, 1 mL) and H2NOH (35 mL, 50 wt. % solution in H2O, 0.53 mol) were added. The suspension was stirred for 7 days at ambient temperature. The mixture was then filtered and dried to the title product (0.20 g, 36%). 1H NMR (400 MHz, DMSO-d6): δ 11.25 (1H, s), 8.95–9.03 (2H, m), 8.83 (1H, s), 8.45 (1H, d, J=8 Hz), 7.05–7.81 (7H, m), 5.78 (2H, s), 2.21 (3H, s). HRMS (M+H)+ found: 332.1400. Calcd for C20H18N3O2: 332.1399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001912B2
Source datasetuspto-grants-2006_02
ORD IDord-f76710a2ee704eb5b9d02c45aa8dfe69
Source noteuspto-grants-2006_02