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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878467Generated: October 31, 2026

Hydroxylamine → HCID 54613496, compound

https://huagongshe.com/reaction/878467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178500251HCID 178500251—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54613496HCID 5461349652.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 7-(5-bromo-1H-benzimidazol-2-yl)heptanoate (100 mg, 0.295 mmol) in THF at 0° C. was added 50% hydroxylamine solution (0.17 mL, 2.70 mmol). To this was added KOH (0.74 mL, 1M in MeOH, 0.74 mmol) dropwise. The reaction was stirred at 0° C. for 2 hr, briefly concentrated and neutralized by adding 1 N HCl solution until pH was 7. The light yellow precipitate was collected by filtration and pump-dried to give 7-(6-bromo-1H-benzimidazol-2-yl)-N-hydroxy heptanamide 15 (53 mg). The filtrate was extracted with ethyl acetate, dried and concentrated. The residue was purified by column to give another portion of the desired product 15 (16 mg). LCMS (M+1@retention time): [email protected] min (LC conditions: 1. Column: YMC, C-18 ODS, 50×4.6 mm 0.5 u; 2. Mobile phase: A 0.05% TFA in water and B 0.05% TFA in acetonitrile; 3. Flow rate 1.2 mL/min; Gradient program: 20% B to 100% B in 3 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987468B2
Source datasetuspto-grants-2015_03
ORD IDord-48a507cc83974632a6cfa7cfdfd79eef
Source noteuspto-grants-2015_03