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HRID 130741作成日:2026年10月26日

Sodium borohydride → 6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamide

https://huagongshe.com/reaction/130741

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物2-CyclopentylethanamineHCID 5305650—
反応物6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
溶媒MethanolHCID 887—
生成物6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamideHCID 5973026152.2%

反応手順

Combine 6-(4-formyl-phenoxy)-nicotinamide (0.61 g, 2.54 mmol) with 2-Cyclopentyl-ethylamine (0.38 g, 3.3 mmol), 2 g of 3 {acute over (Å)} molecular sieves, and 10 mL of methanol. Stir for 18 h under nitrogen. Add sodium borohydride (0.5 g, 13.2 mmol), and stir for 24 h. Filter through Celite, remove the solvent in vacuo. Partition the residue between water (50 mL) and ethyl acetate (100 mL). Dry the organic phase (sodium sulfate), filter, and concentrate in vacuo. Adsorb on silica, and purify on an ISCO® 100 g system (eluting with 95:5:0.5 to 90:10:1 chloroform/ethanol/ammonium hydroxide) to afford 0.45 g of product. HPLC retention time: 5.93 min (98.7% purity), ESMS (M+): 340.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381719B2
出典データセットuspto-grants-2008_06
ORD IDord-84f3d6a721274a9d824451f4301ec669
出典メモuspto-grants-2008_06