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HRID 1037961作成日:2026年10月27日

2-Methyl-2-butene → 2-(1-{[(Tert-butoxy)carbonyl]amino}ethyl)-1,3-thiazole-5-carboxylic acid

https://huagongshe.com/reaction/1037961

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Sodium ChloriteHCID 23668197—
反応物Sodium Phosphate, Monobasic, DihydrateHCID 23673460—
反応物Tert-butyl 1-(5-formylthiazol-2-yl)ethylcarbamateHCID 86657335—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物2-(1-{[(Tert-butoxy)carbonyl]amino}ethyl)-1,3-thiazole-5-carboxylic acidHCID 6739600961.6%

反応手順

A mixture of tert-butyl 1-(5-formylthiazol-2-yl)ethylcarbamate (3.5 g, 0.014 mol), sodium dihydrogen phosphate dihydrate (2.9 g, 0.019 mol) and 2-methyl-2-butene (3.85 g, 0.055 mol) in tert-butyl alcohol (70 ml) and water (40 mL) was stirred at room temperature for 30 minutes. Sodium chlorite (3.22 g, 0.035 mol) was added and the reaction maintained at room temperature for an additional 2 hours. The reaction was concentrated, diluted with water (50 mL) and acidified (pH=4) with the addition of 3N H3PO4. The mixture was extracted with DCM, the organic layer dried over anhydrous Na2SO4 and evaporated to dryness to afford 2-(1-(tert-butoxycarbonylamino)ethyl)thiazole-5-carboxylic acid (2.35 g, 60%). LC-MS: (FA) ES+ 273.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546588B2
出典データセットuspto-grants-2013_10
ORD IDord-4b6996706a9343d78ed403f833a97e5e
出典メモuspto-grants-2013_10