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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895582Generated: October 30, 2026

Hydroxylamine → HCID 22380350, compound

https://huagongshe.com/reaction/895582

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 (s, 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 numberUS06916819B2
Source datasetuspto-grants-2005_07
ORD IDord-31c328d643724adcb48b2a025f0111a9
Source noteuspto-grants-2005_07