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HRID 877366作成日:2026年10月24日

1,2-Dichloroethane → N-[(1R)-1-(5-bromo-1,3-thiazol-2-yl)ethyl]-2-[4-(propan-2-yl)phenyl]acetamide

https://huagongshe.com/ja/reaction/877366

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物4-Isopropylphenylacetic acidHCID 78230—
反応物DiisopropylethylamineHCID 81531—
反応物HOAtHCID 181649—
反応物(1R)-1-(5-bromo-1,3-thiazol-2-yl)ethanamine hydrochlorideHCID 68156351—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-[(1R)-1-(5-bromo-1,3-thiazol-2-yl)ethyl]-2-[4-(propan-2-yl)phenyl]acetamideHCID 69932452—

反応手順

To a solution of 0.050 g (0.28 mmol) 4-isopropylphenyl acetic acid in 0.50 mL DMF and 1.0 mL CH2Cl2 was added 0.072 g (0.30 mmol) (1R)-1-(5-bromo-1,3-thiazol-2-yl)ethanamine hydrochloride, 0.042 g (0.31 mmol) HOAT, 0.059 g (0.31 mmol) EDC, and 0.093 mL (0.56 mmol) DIEA. After 1 h at room temperature, the reaction mixture was purified by preparative reverse-phase HPLC (5->95% CH3CN/H2O over 15 min, 0.05% added TFA, C18) to give N-[(1R)-1-(5-bromo-1,3-thiazol-2-yl)ethyl]-2-[4-(propan-2-yl)phenyl]acetamide. 1H NMR (CDCl3, 400 MHz) δ 7.54 (s, 1H); 7.59 (ABq, J=8.4 Hz, 4H), 6.55 (br d, J=7.6 Hz, 1H), 5.32 (quintet, J=7.2 Hz, 1H), 3.59 (s, 2H), 2.91 (m, J=7.2 Hz, 3H); 1.52 (d, J=7.2 Hz, 3H), 1.25 (d, J=7.2 Hz, 6H). HRMS (ES) [M+1]+ calcd for C16H19BrN2OS: 367.0474. Found: 367.0483.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987310B2
出典データセットuspto-grants-2015_03
ORD IDord-910ab1a7cb984f70a107b865b8fa6a8e
出典メモuspto-grants-2015_03