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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N',N'',N''-Hexamethylmethanetriamine | HCID 79831 | — |
| Reactant | Hydrazine, acetate (1:1) | HCID 165591 | — |
| Reactant | HCID 22379891 | HCID 22379891 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178462501 | HCID 178462501 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916819B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-46aa61c393d84c23ba96c182990e6ccb |
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| Source note | uspto-grants-2005_07 |
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