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HRID 131657作成日:2026年10月27日

2-Tetralone → 2-(S)-(1,2,3,4-Tetrahydro-naphthalen-2-ylamino)-pentanoic acid (5-isopropyl-thiazol-2-yl)-amide

https://huagongshe.com/reaction/131657

反応式

関与物質

役割名称HCID仕込み量
反応物2-TetraloneHCID 68266—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-(S)-amino-pentanoic acid (5-isopropyl-thiazol-2-yl)amideHCID 86604587—
触媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
生成物2-(S)-(1,2,3,4-Tetrahydro-naphthalen-2-ylamino)-pentanoic acid (5-isopropyl-thiazol-2-yl)-amideHCID 11610411—

反応手順

A mixture of 2-(S)-amino-pentanoic acid (5-isopropyl-thiazol-2-yl)-amide (350 mg, 1.4 mmol) and 2-tetralone (318 mg, 2.2 mmol)in 20 mL of methylene chloride and 5 drops of acetic acid was treated with sodium triacetoxyborohydride (462 mg, 2.2 mmol) and stirred at room temperature overnight. The mixture was concentrated and eluted through SPEC SCX cartridge and concentrated to dryness. The residue was purified by silica gel column chromatography to give 2-(S)-(1,2,3,4-Tetrahydro-naphthalen-2-ylamino)-pentanoic acid (5-isopropyl-thiazol-2-yl)-amide as a solid, LC-MS, RT=1.9 min, M+1=372.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384968B2
出典データセットuspto-grants-2008_06
ORD IDord-e16c27bbe9224dc3992a6a93e3689b5c
出典メモuspto-grants-2008_06