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HRID 1917581作成日:2026年10月25日

Triethylamine → 6,6-Dimethyl-3-(5-(phenylethynyl)pyrazin-2-yl)-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1917581

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TriphosgeneHCID 94429—
反応物2-Methyl-4-(5-phenylethynyl-pyrazin-2-ylamino)-butan-2-olHCID 57516784—
溶媒TetrahydrofuranHCID 8028—
生成物6,6-Dimethyl-3-(5-(phenylethynyl)pyrazin-2-yl)-1,3-oxazinan-2-oneHCID 5349470072%

反応条件

温度2.5 °C

反応手順

A solution of 2-methyl-4-(5-(phenylethynyl)pyrazin-2-ylamino)butan-2-ol (Example 168, step 2) (84 mg, 0.30 mmol) and triethylamine (91 mg, 125 μl, 0.90 mmol, 3 equiv.) in 2 ml of THF was cooled to 0-5° C. and triphosgene (89 mg, 0.30 mmol, 1 equiv.) was added in portions. The mixture was stirred for 1 hr at 0-5° C. and for 2 hours at room temperature. The reaction mixture was quenched with saturated sodium carbonate solution followed by workup with ethyl acetate/water. The organic layers were combined, dried and concentrated. The crude product was chromatographed over a prepacked 20 g Silica column eluting with a heptane to 50% ethyl acetate in heptane gradient to yield the title compound (66.1 mg, 72% yield) as an off-white solid, MS: m/e=308.3 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618296B2
出典データセットuspto-grants-2013_12
ORD IDord-ffbadfb089f94a858de600e83ea3a43c
出典メモuspto-grants-2013_12