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HRID 41159作成日:2026年10月26日

Triethylamine → (1S,2S,4R)-2-methoxy-4-(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)cyclopentyl nitrate

https://huagongshe.com/reaction/41159

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Semicarbazide hydrochlorideHCID 11236—
反応物Sodium HydroxideHCID 14798—
反応物Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
反応物(1S,2S,4R)-4-carbamoyl-2-methoxycyclopentyl nitrateHCID 58443610—
溶媒DichloromethaneHCID 6344—
生成物(1S,2S,4R)-2-methoxy-4-(5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)cyclopentyl nitrateHCID 136164176—

反応手順

(1S,2S,4R)-4-carbamoyl-2-methoxycyclopentyl nitrate (example 14, 0.14 g, 0.68 mmol) and bis(2-oxo-3-oxazolidinyl)phosphinic chloride (0.19 g, 0.75 mmol) were stirred for 10 minutes in dichloromethane (5 mL) and triethylamine (0.29 mL, 2.1 mmol). Semicarbazide hydrochloride (0.082 g, 0.73 mmol) was added and stirred at room temperature for 4 days. The solution was concentrated in vacuo and brought up in 1 M sodium hydroxide (3 mL, 3.0 mmol) to reflux for 8 hours. Purification of the crude product by reversed-phase mass-directed high-performance liquid chromatography afforded the title compound as a colorless liquid. 1H NMR (500 MHz, CDCl3) δ 1.93-1.98 (m, 1H), 2.34 (dd, J=4.1, 8.3 Hz, 2H), 2.40-2.47 (m, 1H), 2.40-2.47 (m, 1H), 3.42 (quintet, J=6.2 Hz, 1H), 3.50 (s, 3H), 3.93-3.96 (m, 1H), 5.40-5.43 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530521B2
出典データセットuspto-grants-2013_09
ORD IDord-22e3c288424f496b8bb664fc6edef27d
出典メモuspto-grants-2013_09