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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895583Generated: October 29, 2026

N,N,N',N',N'',N''-Hexamethylmethanetriamine → HCID 178462501, compound

https://huagongshe.com/reaction/895583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N',N'',N''-HexamethylmethanetriamineHCID 79831—
ReactantHydrazine, acetate (1:1)HCID 165591—
ReactantHCID 22379891HCID 22379891—
SolventEthanolHCID 702—
ProductHCID 178462501HCID 178462501—

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. EtOH (5 mL) and hydrazine acetate (1.1 mmol) are added to the residue. The mixture is heated at 120° C. for 2 hours. The solvent is removed. NaHCO3 (aq.) (10 mL) and DCM (30 mL) are added to the residue. 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)-1H-pyrazol-4-ylmethyl]-1H-benzoimidazole as a solid. LRMS: calcd 399.3, found [M+1] 401.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916819B2
Source datasetuspto-grants-2005_07
ORD IDord-46aa61c393d84c23ba96c182990e6ccb
Source noteuspto-grants-2005_07