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HRID 726719作成日:2026年10月26日

Hydrochloric Acid → 3-[4-Cyanobenzyl]aminopropanoic acid

https://huagongshe.com/reaction/726719

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-CyanobenzaldehydeHCID 66042—
反応物Ethyl 3-aminopropanoateHCID 419889—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Lithium hydroxide methanolHCID 23717829—
溶媒Acetic AcidHCID 176—
溶媒DimethylformamideHCID 6228—
生成物3-[4-Cyanobenzyl]aminopropanoic acidHCID 1676998779%

反応手順

4-cyanobenzaldehyde (0.65 g; 5 mmoles) and β-alanine ethyl ester.HCl (0.76 g; 5 mmoles) were dissolved in N,N-dimethylformamide (10 ml) containing 1% acetic acid. After 10 min., sodiumcyanoborohydride (0.35 g; 5 mmoles) was added to the solution. The reaction mixture was stirred at room temperature for 12 hrs. and taken down to dryness under reduced pressure. The residue was treated with 1N lithium hydroxide/methanol (1:1; 20 ml) for 15 min. Methanol was removed and the pH of the remaining solution was adjusted to pH 5 with 50% acetic acid. The product was purified by HPLC using a linear gradient of acetonitrile/water/trifluoroacetic acid. The desired fractions was collected and lyophilized to give 0.81 g of white solid (79% yield). FAB-MS: MH+ =205.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05710166
出典データセットuspto-grants-1998_01
ORD IDord-c6ad0981756643088329bfd4623ad976
出典メモuspto-grants-1998_01