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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203336Generated: October 31, 2026

Methanol → 6-chloro-1-(3,3,4,4,4-pentafluorobutyl)-1H-indazole-3-carboximidamide

https://huagongshe.com/reaction/2203336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
Reactant6-chloro-1-(3,3,4,4,4-pentafluorobutyl)-1H-indazole-3-carbonitrileHCID 86678972—
SolventTolueneHCID 1140—
Product6-chloro-1-(3,3,4,4,4-pentafluorobutyl)-1H-indazole-3-carboximidamideHCID 86678973—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trimethylaluminum (2.0M in toluene, 23.17 mL, 46.3 mmol) was added dropwise to a suspension of ammonium chloride (2.49 g, 46.5 mmol) in 69 mL toluene cooled to 0° C. The solution was then stirred at room temperature for 3 hours. This solution was then added to the intermediate from Step D (3.0 g, 9.27 mmol) and then heated at 110° C. for 6 hours. The solution was then cooled to room temperature and carefully poured to silica gel (ca 150 mL) and methanol (ca 250 mL). After stirring for 1.5 hours the suspension was filtered and the filtrate concentrated to give the indicated product which was used in the next step without further purification. 1H NMR (400 MHz, CH3 CN-d3): selected peaks δ 8.26 (d, J=8.7 Hz, 1H); 7.70 (d, J=1.7 Hz, 1H); 7.24 (dd, J=8.7, 1.8 Hz, 1H); 4.67 (t, J=7.1 Hz, 2H); 3.01-2.78 (m, 2H). m/z=341.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-9bc9e40a70744e8ab280d24edf3bc4e2
Source noteuspto-grants-2016_06