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HRID 1396478作成日:2026年10月27日

Trifluoroacetic acid → 6-Bromo-5-fluoropyridin-2-amine

https://huagongshe.com/reaction/1396478

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Tert-butyl (6-bromo-5-fluoropyridin-2-YL)carbamateHCID 71744124—
溶媒DichloromethaneHCID 6344—
生成物6-Bromo-5-fluoropyridin-2-amineHCID 5960583391%

反応手順

To a solution of (6-bromo-5-fluoro-pyridin-2-yl)-carbamic acid tert-butyl ester (1.43 g, 4.91 mmol) in DCM (25 mL) was added TFA (3.78 mL, 49.1 mmol, Eq: 10.0). The mixture was stirred at room temperature for 2 h, after which it was concentrated in vacuo, and redissolved in EtOAc. The organic layer was washed with sat. aq. NaHCO3 followed by water and brine. The resulting organic layer was concentrated on to silica gel and chromatographed (10% to 40% EtOAc/hexanes) to give 6-bromo-5-fluoro-pyridin-2-ylamine (850 mg, 91%). 1H NMR (400 MHz, CHLOROFORM-d6) δ ppm 7.23 (dd, J=8.6, 7.5 Hz, 1H), 6.41 (dd, J=8.6, 2.6 Hz, 1H), 4.40 (br. s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08901124B2
出典データセットuspto-grants-2014_12
ORD IDord-cc36f01cdd014233bd45c2777bbfdcf9
出典メモuspto-grants-2014_12