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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722121Generated: October 30, 2026

Hydroxylamine → HCID 3013462, compound

https://huagongshe.com/reaction/722121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantEthyl Beta-Carboline-3-CarboxylateHCID 105078—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 3013462HCID 301346239.1%

Reaction Steps

To a stirred solution of ethyl 9H-β-carboline-3-carboxylate (290 mg, 1.21 mmol) in DMF (4 mL) under a nitrogen atmosphere was added NaH (53 mg, 60% in mineral oil, 1.33 mmol) portionwise, followed by benzyl bromide (173 μL, 1.45 mmol). Stirring was continued for 21 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 (25 mL). To the resulting solution, H2NOH (25 mL, 50 wt. % solution in H2O, 0.38 mol) was added. The suspension was stirred for 3 days at ambient temperature. The mixture was then filtered, and the solid was boiled in methanol (25 mL). After filtration, the title product (0.15 g, 39%) was obtained. 1H NMR (400 MHz, DMSO-d6): δ 11.32 (1H, s), 9.10 (1H, s), 9.05 (1H, s), 8.89 (1H, s), 8.52 (1H, d, J=8 Hz), 7.26–7.87 (8H, m), 5.90 (2H, s). HRMS (M+H)+ found: 318.1249. Calcd for C19H16N3O2: 318.1243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138408B2
Source datasetuspto-grants-2006_11
ORD IDord-ba013fc8297c4df5a4441018853493b3
Source noteuspto-grants-2006_11