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HRID 408590作成日:2026年10月27日

Sulfuric acid magnesium salt (1:1) → 4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester

https://huagongshe.com/reaction/408590

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Sodium borohydrideHCID 4311764—
反応物4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
反応物Benzofuran-6-carbaldehydeHCID 14354086—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl esterHCID 70556474—

反応条件

温度20 °C

反応手順

To a solution of 4-amino-butyric acid ethyl ester hydrochloride (1 eq.) in THF was added TEA (2.5 eq.). The mixture was stirred 5 min at 20° C., then benzofuran-6-carbaldehyde (0.95 eq.) and MgSO4 (3 eq.) were added. The reaction was refluxed for 2 h, then cooled to 20° C. and filtered. The filtrate was added to a suspension of NaBH4 (2 to 6 eq.) in MeOH at −15° C. The reaction was stirred for 2 h at −15° C. The reaction was quenched with the addition of aqueous HCl 2N until pH=2. The aqueous layer was washed twice with EtOAc. The organic layers were discarded. Solid KOH was added to the aqueous layer. The crude was extracted three times with EtOAc. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure at 20° C. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 95/5) to afford 4-[(benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759334B2
出典データセットuspto-grants-2014_06
ORD IDord-ac60bff47ab3460f836ac051f1ee32e2
出典メモuspto-grants-2014_06