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HRID 541572作成日:2026年10月27日

Triethylamine → Tert-butyl{3-[(2-methoxy-5-nitrophenyl)ethynyl]phenyl}carbamate

https://huagongshe.com/reaction/541572

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Iodo-1-methoxy-4-nitrobenzeneHCID 94806—
反応物tert-Butyl 3-ethynylphenylcarbamateHCID 11275982—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl{3-[(2-methoxy-5-nitrophenyl)ethynyl]phenyl}carbamateHCID 5796166640%

反応条件

温度80 °C

反応手順

tert-Butyl (3-ethynylphenyl)carbamate was stirred with 2-iodo-1-methoxy-4-nitrobenzene (2.60 g, 9.31 mmol) and bis(triphenylphosphine)palladium(II) chloride (163 mg, 0.23 mmol) in N,N-dimethylformamide (15 mL), and triethylamine (2.59 mL, 18.6 mmol) was added. The reaction mixture was heated at 80° C. for 15 minutes. Purification by preparative LCMS (pH 10) gave the desired compound (1.38 g, 40%). 1H NMR (300 MHz, DMSO-d6): δ 9.53 (s, 1H), 8.25 (m, 2H), 7.71 (s, 1H), 7.42 (d, 1H), 7.25 (m, 2H), 7.18 (d, 1H), 4.00 (s, 3H), 1.42 (s, 9H). LCMS for C20H21N2O5 (M+H)+: m/z=369.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871753B2
出典データセットuspto-grants-2014_10
ORD IDord-974a337b796049089504cf9eeee21670
出典メモuspto-grants-2014_10