Butylamine → Terbinafine Hydrochloride

To 33 ml of tetrahydrofuran were added 5.40 g (22 mmol) of (E)-N-(3-chloro-2-propenyl)-N-methyl-1-naphthalenemethanamine, 210 mg (1.1 mmol) of copper (I) iodide and 356 mg (0.31 mmol) of tetrakis (triphenylphosphine)palladium, and further, 4.35 ml (44 mmol) of n-butylamine and 2.83 ml (23.1 mmol) of tert-butylacetylene under ice cooling. The mixture was stirred for 17 hours at room temperature. The reaction mixture was concentrated and the residue was subjected to silica gel chromatography (n-hexane→n-hexane/ethyl acetate=9/1→4/1). The desired fractions were put together and concentrated under reduced pressure. The oily residue was dissolved in 6 ml of ethanol and 6 ml of 23% hydrogen chloride methanol solution was added thereto. The solvent and excess hydrogen chloride were distilled off. The resulting crystals were suspended in diisopropyl ether, filtered, washed with diisopropyl ether and dried to obtain 6.41 g (yield: 89%) of the above identified compound as white crystalline powder.

1. concentrationThe reaction mixture was concentrated
2. concentrationconcentrated under reduced pressure
3. dissolutionThe oily residue was dissolved in 6 ml of ethanol
4. addition6 ml of 23% hydrogen chloride methanol solution was added
5. distillationThe solvent and excess hydrogen chloride were distilled off
6. filtrationfiltered
7. washwashed with diisopropyl ether
8. customdried
9. customto obtain 6.41 g (yield: 89%) of the

ORDレコード

ord-3a6398c8ca134856b3af144348d8ccab

出典データセット

uspto-grants-1993_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05231183