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HRID 555585作成日:2026年10月26日

4-Hydroxybenzoic Acid → 4-hydroxy-benzoic acid, compd. with (2S,4E)-N-methyl-5-[5-(1-methylethoxy)-3-pyridinyl]-4-penten-2-amine (1:1)

https://huagongshe.com/reaction/555585

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxybenzoic AcidHCID 135—
反応物IsopropanolHCID 3776—
反応物IsproniclineHCID 9824145—
溶媒Isopropyl AcetateHCID 7915—
生成物4-hydroxy-benzoic acid, compd. with (2S,4E)-N-methyl-5-[5-(1-methylethoxy)-3-pyridinyl]-4-penten-2-amine (1:1)HCID 11552485—

反応手順

p-Hydroxybenzoic acid (2.62 g, 19.0 mmol) was added in portions to a stirred solution (2S)-(4E)-N-methyl-5-(5-isopropoxy-3-pyridinyl)-4-penten-2-amine (4.79 g of 93% pure, 19.0 mmol) in isopropyl acetate (50 mL). During the addition, crystallization of salt was evident. After complete addition of the p-hydroxybenzoic acid, the suspension was heated near its boiling point as isopropanol was slowly added. After 15 mL of isopropanol had been added, complete dissolution was obtained. Cooling of the solution to ambient temperature (overnight) resulted in deposition of a crystalline mass, which was collected by suction filtration and air dried (4.03 g). A second crop (0.82 g) was isolated from the concentrated filtrate, by addition of acetone. The two crops of crystals were combined and recrystallized from acetone (50 mL). The solid was collected by suction filtration and dried in the vacuum oven (50° C.) for 18 h. This left 4.24 g (60.0%) of white crystals (98+% pure by both GCMS and LCMS; m.p. 99-101° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053451B2
出典データセットuspto-grants-2011_11
ORD IDord-b703e66c9f7d46429d95d22b6ffc5b02
出典メモuspto-grants-2011_11