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HRID 79116作成日:2026年10月25日

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(2-bromothiazole-4-carbonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/79116

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-Bromo-1,3-thiazole-4-carboxylic acidHCID 2763209—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(2-bromothiazole-4-carbonyl)piperazine-1-carboxylateHCID 5829978492.8%

反応条件

温度20 °C

反応手順

2-bromothiazole-4carboxylic acid (1.31 g, 6.3 mmol) was combined with tert-butyl piperazine-1-carboxylate (1.2 g, 6.3 mmol) in DCM (15 mL), and then stirred at 20° C. until it formed a clear solution. N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (1.2 g, 6.3 mmol) was then added, and the reaction was stirred at 20° C. for 2 hours. The reaction was concentrated in vacuum, before transferring it to a separation funnel with ethyl acetate. The organic layer was washed with saturated NaHCO3, water, NH4Cl, and then with brine. After drying the organic layer with MgSO4, it was concentrated in vacuum to yield compound 72 (2.2 g, 91%) as a light yellow solid. 1H NMR (500 MHz, DMSO-d6) δ 8.16 (1H, s), 3.61 (4H, m), 3.38 (4H, m), 1.42 (9H, s) ppm; LCMS-ESI (POS), M/Z, M+1-C3H9: Found 320.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841312B2
出典データセットuspto-grants-2014_09
ORD IDord-28eac06b7a984ea8950dc23d30f3b495
出典メモuspto-grants-2014_09