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HRID 483751作成日:2026年10月25日

Benzamide → N-[(3S,4R)-3-Hydroxy-2,2-dimethyl-6-(trifluoromethoxy)-chroman-4-yl]-2-nitrobenzamide

https://huagongshe.com/reaction/483751

反応式

関与物質

役割名称HCID仕込み量
反応物BenzamideHCID 2331—
反応物TriethylamineHCID 8471—
反応物2-Nitrobenzoyl chlorideHCID 11875—
反応物(3S,4R)-4-Amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-olHCID 15020328—
溶媒DichloromethaneHCID 6344—
生成物N-[(3S,4R)-3-Hydroxy-2,2-dimethyl-6-(trifluoromethoxy)-chroman-4-yl]-2-nitrobenzamideHCID 6775442647%

反応条件

温度15 °C

反応手順

(3S,4R)-4-Amino-2,2-dimethyl-6-(trifluoromethoxy)-chroman-3-ol [prepared by the method of Quagliato et al. Biorg. & Med. Chem. Let. 1991 1, 39; (2.75 g, 10 mmol)] and triethylamine (1.39 mL, 10 mmol) were stirred together in dichloromethane (25 mL) at 0° C. To this solution was added a solution of 2-nitrobenzoylchloride (1.32 mL, 10 mmol) in dichloromethane (10 mL). The ice bath was allowed to gradually warm to 15° C. overnight. The crude benzamide was diluted with dichloromethane (50 mL), washed with water (2×10 mL), dried (MgSO4) and concentrated to afford 2.0 g (47%) of white solid: m.p. 189°-190° C.; 1H NMR (DMSO-d6): δ 9.17 (d, 1H), 8.04 (d, 1H), 7.81 (m, 2H), 7.71 (t, 1H), 7.33 (s, 1H), 7.16 (d, 1H), 6.86 (d, 1H), 5.86 (d, 1H), 4.96 (br t, 1H), 3.64 (dd, 1H), 1.42 (s, 3H), 1.19 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225566
出典データセットuspto-grants-1993_07
ORD IDord-049b58c31cb74babb9ed19ecf0e1584f
出典メモuspto-grants-1993_07