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HRID 72403作成日:2026年10月25日

Diisopropylethylamine → tert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/72403

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylateHCID 21306970879.8%

反応手順

A mixture of 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid (D25) (5 g, 24.85 mmol), 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (14.39 g, 75.55 mmol), 1-hydroxybenzotriazole hydrate (0.38 g, 2.48 mmol) and N,N-diisopropylethylamine (34.6 ml, 198 mmol) in dimethylformamide (80 ml) was stirred overnight at room temperature. The reaction mixture was then concentrated to half volume in vacuo, poured into water (60 ml) and extracted with ethylacetate (3×60 ml). The combined organic phases were washed with saturated aqueous NH4Cl (100 ml), saturated aqueous NaHCO3 (100 ml), water and brine (100 ml), dried with Na2SO4 anhydrous (50 g) and concentrated under reduced atmosphere. Collected organics after solvent evaporation afforded the title compound (D26) (5.33 g)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828987B2
出典データセットuspto-grants-2014_09
ORD IDord-42b3c6e45f714d7a89c6106a2a386ac7
出典メモuspto-grants-2014_09