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HRID 60645作成日:2026年10月24日

Triethylamine → 5-tert-Butyl-2-(3-methyl-5-triisopropylsilanyloxy-phenyl)-2H-pyrazol-3-ylamine

https://huagongshe.com/ja/reaction/60645

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
反応物3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-5-methyl-phenolHCID 117729587—
溶媒DichloromethaneHCID 6344—
生成物5-tert-Butyl-2-(3-methyl-5-triisopropylsilanyloxy-phenyl)-2H-pyrazol-3-ylamineHCID 123301916105.3%

反応手順

To a solution of Intermediate 54a (430 mg, 1.75 mmol) in DCM (10 mL) and triethylamine (0.36 mL, 2.63 mmol) was added triisopropylsilyltrifluoromethanesulphonate (0.52 mL, 1.93 mmol). Mixture stirred for 1 h at RT, diluted with DCM, washed with sat. sodium hydrogen carbonate solution then brine, dried, and concentrated in vacuo. The residue was purified by FCC, using 0-25% EtOAc in cyclohexane, to give impure title compound (740 mg), contaminated with the ˜25% bis-silyl impurity. 1H NMR (300 MHz, CDCl3): inter alia 1.03-1.15 (18H, m), 1.18-1.35 (12H, m), 2.32 (3H, s), 3.74 (2H, br s), 5.49 (1H, s), 6.60-6.66 (1H, m), 6.85-6.89 (1H, m), 6.95-7.00 (1H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440974B2
出典データセットuspto-grants-2016_09
ORD IDord-51ff804b18514e8f88612bc06140232b
出典メモuspto-grants-2016_09