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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784963Generated: October 30, 2026

1-Methylpiperazine → HCID 178481024, compound

https://huagongshe.com/reaction/1784963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 178477904HCID 178477904—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178481024HCID 17848102422.4%

Reaction Steps

To a suspension of 5-chloro-2-trichloromethyl-1H-benzoimidazole (100 mg, 0.37 mmol) in acetonitrile (4 mL) was added N-methylpiperazine (0.04 mL, 0.4 mmol). The mixture was stirred for 10 min then ammonium acetate (29 mg, 0.38 mmol) was added. After 18 h the reaction mixture was diluted with satd aq NaHCO3 (10 mL), and then extracted with dichloromethane (3×10 mL). The combined extracts were dried (Na2SO4) and then concentrated under reduced pressure. The crude product was purified on silica gel (10 g; 0-10% methanol (2 M NH3)/dichloromethane) to afford 23 mg (22%) of the title compound. MS (ESI): mass calculated for C13H16N4O, 277.11; m/z found, 278.2 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.79-7.74 (m, 2H)1 7.45 (dd, J=8.6, 2.0 Hz, 1H), 4.23-4.17 (m, 4H), 3.63-3.58 (m, 4H), 3.01 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504426B2
Source datasetuspto-grants-2009_03
ORD IDord-684e4a3330224d4e9dccb562656e8dbc
Source noteuspto-grants-2009_03