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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891015Generated: October 30, 2026

Hydroxylamine → HCID 3013461, compound

https://huagongshe.com/reaction/891015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantSodium hydrideHCID 24758—
ReactantEthyl Beta-Carboline-3-CarboxylateHCID 105078—
Reactant1-(Bromomethyl)-3-chloro-2-fluorobenzeneHCID 522827—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 3013461HCID 301346131%

Reaction Steps

To a stirred solution of ethyl 9H-β-carboline-3-carboxylate (400 mg, 1.66 mmol) in DMF (5 mL) under nitrogen atmosphere was added NaH (66.4 mg, 60% in mineral oil, 1.66 mmol) portionwise, followed by 3-chloro-2-fluoro-benzyl bromide (371 mg, 1.66 mmol). Stirring was continued for 25 hours at ambient temperature, water (30 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 4 days at ambient temperature. The mixture was then filtered, and the solid was boiled in methanol (20 mL). After filtration, the title product (0.19 g, 31%) was obtained. 1H NMR (400 MHz, DMSO-d6): δ 11.33 (1H, s), 9.08 (1H, s), 9.04 (1H, s), 8.89 (1H, s), 8.51 (1H, d, J=8 Hz), 6.95–7.81 (6H, m), 6.00 (2H, s). HRMS (M+H)+ found: 370.0764. Calcd for C19H14N3O2FCl: 370.0759.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001912B2
Source datasetuspto-grants-2006_02
ORD IDord-99d54d60adfb4085bdc8843b83d4aa10
Source noteuspto-grants-2006_02