반응 #970316

반응 방정식

2-amino-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide

triethylamine

4-bromobutanoyl chloride

→

title compound

수율 92.0%

2-(4-bromobutanamido)-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide

수율 92.0%

용매

dichloromethane

tetrahydrofuran

dichloromethane

반응 조건

후처리

1. 1
   세척washed with saturated aqueous sodium bicarbonate solution (2×150 mL), and brine (150 mL)
2. 2
   건조The organic layer was dried over anhydrous sodium sulfate
3. 3
   여과filtered
4. 4
   농축the filtrate was concentrate in vacuo

실험 절차

To a solution of 2-amino-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide (5.60 g, 22.0 mmol) and triethylamine (2.61 g, 26.0 mmol) in anhydrous tetrahydrofuran (250 mL) was added 4-bromobutanoyl chloride (4.99 g, 26.0 mmol) in anhydrous dichloromethane (10 mL) dropwise at 0° C. The reaction mixture was stirred at ambient temperature for 2 hours, then diluted with dichloromethane (200 mL) and washed with saturated aqueous sodium bicarbonate solution (2×150 mL), and brine (150 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrate in vacuo to afford the title compound as a yellow oil in 92% yield (8.00 g): 1H NMR (300 MHz, CDCl3) δ 8.61 (br s, 1H), 7.32-7.22 (m, 2H), 7.05-6.94 (m, 2H), 6.14 (t, J=5.6 Hz, 1H), 4.53 (d, J=5.6 Hz, 2H), 3.45 (t, J=6.7 Hz, 2H), 2.65 (t, J=6.7 Hz, 2H), 2.58 (s, 3H), 2.23 (quintet, J=6.7 Hz, 2H); MS (ES+) m/z 413.1 (M+1), 415.1 (M+1).

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