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HRID 2277503作成日:2026年10月26日

(Cyclopropylmethyl)methylamine → US10273222, Example 59

https://huagongshe.com/reaction/2277503

反応式

関与物質

役割名称HCID仕込み量
反応物(Cyclopropylmethyl)methylamineHCID 12919209—
反応物methyl 2-(1-{2-[(methylsulfonyl)oxy]ethyl}-1H-imidazol-4-yl)pyridine-4-carboxylateHCID 90407071—
溶媒TolueneHCID 1140—
生成物US10273222, Example 59HCID 9040746334.4%

反応手順

A solution of methyl 2-(1-{2-[(methylsulfonyl)oxy]ethyl}-1H-imidazol-4-yl)pyridine-4-carboxylate (100 mg, 0.31 mmol) and cyclopropylmethyl(methyl)amine (260 mg, 3.1 mmol) in toluene (5 mL) was heated at 110° C. in a sealed tube for 24 hrs. The solution was concentrated to an oily residue which was dissolved in MeOH (5 mL). To this solution was added 10 N NaOH solution (1 g). The mixture was stirred and refluxed for 1 hr and then cooled to RT. The pH was carefully adjusted to 6.5 and the resulting mixture was concentrated to a residue. The residue was diluted with MeOH (10 mL) and filtered. The solids were washed with additional MeOH (10 mL). The filtrate was concentrated to an oily residue and chromatographed on silica gel (90% MeOH, 10% pH 7 buffer [potassium phosphate based] to give a foam. The foam was then chromatographed on reverse phase C18 silica gel [40-63 microns (mesh 230-400); 60 Å; 500 m2/g; pore volume 0.8 ml/g] using 80% MeOH/10% DI H2O to give the title compound (32 mg) as a beige solid: 1HNMR (400 MHz, CD3OD): δ 0.29 (2H, s), 0.73 (2H, s), 1.05 (1H, m), 2.77 (5H, m), 3.51 (2H, t, J=4.2 Hz), 4.45 (2H, t, J=4.2 Hz), 7.79 (1H, s), 7.92 (2H, m), 8.43 (1H, s), 8.64 (1H, s). [M+H] Calc'd for C16H20N4O2, 301. Found, 301.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09133166B2
出典データセットuspto-grants-2015_09
ORD IDord-bf19ccc85b274c8dbd1142d1eb3a7132
出典メモuspto-grants-2015_09