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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907195Generated: November 3, 2026

Formamidine acetate → HCID 178432631, compound

https://huagongshe.com/reaction/1907195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
Reactant4-(5-bromo-1-methyl-1H-pyrazol-4-yl)-2-methyl-1H-imidazol-1-amine, trifluoroacetate saltHCID 131731061—
Solvent(+-)-2-ButanolHCID 6568—
ProductHCID 178432631HCID 178432631—

Reaction Conditions

Temperature100 °C

Reaction Steps

4-(5-Bromo-1-methyl-1H-pyrazol-4-yl)-2-methyl-1H-imidazol-1-amine, trifluoroacetate salt (4.90 g, 113.2 mmol) was combined with formamidine acetate (98%, 4.92 g, 46.3 mmol) in 2-butanol (40 mL), and the reaction mixture was heated at 100° C. for 6 hours, then allowed to cool to room temperature and stir for 18 hours. The off-white solid was collected by filtration and washed with 2-propanol followed by diethyl ether. The solid was then triturated with aqueous ammonium hydroxide (7.5 M, 40 mL); filtration provided a white solid, which was washed with 2-propanol followed by diethyl ether to provide the product. Yield: 2.70 g, 9.54 mmol, 72%. 1H NMR (500 MHz, CD3OD), presumed to be a mixture of rotamers or tautomers: δ 2.26 and 2.31 (2 s, 3H), 3.89 and 3.89 (2 s, 3H), 7.26 and 7.40 (2 s, 1H), 7.41 and 7.96 (2 br s, 1H), 7.85 and 7.82 (2 s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598155B2
Source datasetuspto-grants-2013_12
ORD IDord-7fd1be415d40403887c1bf8ad874eee3
Source noteuspto-grants-2013_12