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HRID 272697作成日:2026年10月26日

4-Methyl-5-(2-hydroxyethyl)thiazole → 4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroaniline

https://huagongshe.com/reaction/272697

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
反応物TriphenylphosphineHCID 11776—
反応物Di-tert-butyl azodicarboxylateHCID 97268—
反応物4-Amino-3-NitrophenolHCID 3758882—
溶媒TetrahydrofuranHCID 8028—
生成物4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroanilineHCID 6921998386.2%

反応手順

A mixture of 4-amino-3-nitrophenol (386 mg, 2.5 mmol), 2-(4-methyl-1,3-thiazol-5-yl)ethanol (0.299 mL, 2.5 mmol), polymer supported triphenylphosphine (1.25 g, 3 mmol/g, 3.75 mmol), and di-tert-butyl azodicarboxylate (864 mg, 3.75 mmol) in THF (10 mL) was stirred at room temperature for 16 hours. Filtered through Celite and concentrated under vacuum. The residue was purified by flash column chromatography on silica gel with 1:1 hexanes/ethyl acetate to provide 602 mg (86%) of the desired product. MS (DCI) m/e 279 (M+H)+, 1H NMR (300 MHz, DMSO-d6): □ 8.83 (s, 1H), 7.37 (d, J=3.05 Hz, 1H), 7.25 (s, 2H), 7.16 (dd, J=8.99, 2.88 Hz, 1H), 7.01 (s, 1H), 4.10 (t, J=6.27 Hz, 2H), 3.19 (t, J=6.27 Hz, 2H), 2.35 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456169B2
出典データセットuspto-grants-2008_11
ORD IDord-409df72e33cf45d8a976a3b4eefceee5
出典メモuspto-grants-2008_11