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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594112Generated: October 31, 2026

Hydroxylamine → HCID 22380350, compound

https://huagongshe.com/reaction/1594112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantN,N,N',N',N'',N''-HexamethylmethanetriamineHCID 79831—
ReactantHCID 22379891HCID 22379891—
SolventEthanolHCID 702—
ProductHCID 22380350HCID 22380350—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-(5-Bromo-1-ethyl-1H-benzoimidazol-2-yl)-1-(3-fluoro-phenyl)-propan-1-one (0.1 g, 0.27 mmol) and tris(dimethylamino)methane (0.077 g, 0.54 mmol) is heated at 60° C. in a sealed tube for 6 hours. The volatile material is removed in vacuo. To the residue is added EtOH (5 mL) and hydroxylamine (1.1 mmol). The mixture is heated at 120° C. for 2 hours. The solvent is removed. To the residue is added NaHCO3 (aq.) (10 mL) and DCM (30 mL). The organic layer is separated and the aqueous layer is extracted with DCM (2×15 mL). The combined organic layers are dried and the solvent removed. The crude is purified by PTLC (ethyl acetate/Hexanes 1:1) to give 5-Bromo-1-ethyl-2-[3-(3-fluoro-phenyl)-isoxazol-4-ylmethyl]-1H-benzoimidazole as a solid. 1H NMR (CDCl3) δ 8.40 (3, 1H), 7.88 (s, 1H), 7.31-7.52 (m, 4H), 7.18-7.22 (m, 2H), 4.14 (s, 2H), 4.04 (q, 2H), 1.18 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300945B2
Source datasetuspto-grants-2007_11
ORD IDord-2ecf4880b42c491e9595e229eaf6c762
Source noteuspto-grants-2007_11