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HRID 521613作成日:2026年10月24日

Triethylamine → HCID 57814706、化合物

https://huagongshe.com/ja/reaction/521613

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-acetyl-L-methionineHCID 448580—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物N-(4-(2-aminoethoxy)-3-(1-methyl-1H-pyrazol-5-yl)phenyl)-3-methoxybenzamide hydrochlorideHCID 67265457—
溶媒DichloromethaneHCID 6344—
生成物HCID 57814706HCID 5781470657.3%

反応手順

(S)-2-acetamido-4-(methylthio)butanoic acid (17.8 mg, 1.25 eq), triethylamine (20.8 mL, 2.0 eq) and HATU (35.4 mg, 1.25 eq) were dissolved in 3 mL of dichloromethane and stirred at room temperature for 10 minutes. At this time N-(4-(2-aminoethoxy)-3-(1-methyl-1H-pyrazol-5-yl)phenyl)-3-methoxybenzamide hydrochloride (30 mg, 74.5 μmol) dissolved in 2.0 mL of dichloromethane was added and the reaction was stirred at room temperature for 3 hr. The solvents were evaporated under a stream of nitrogen and it was purified by HPLC. The proper fractions were collected and lyophilized to afford the title compound as a white solid in 57.3% yield. LCMS m/z (%)=540 (M+H, 100). 1H NMR (400 MHz, CDCl3) δ ppm 2.01 (s, 4H), 2.07 (s, 3H), 2.38-2.44 (m, 2H), 3.46-3.65 (m, 2H), 3.85 (s, 3H), 3.88 (s, 3H), 4.03-4.12 (m, 2H), 4.45-4.53 (m, 1H), 6.39 (d, J=2.02 Hz, 1H), 7.02 (d, J=9.60 Hz, 1H), 7.11 (dt, J=4.80, 2.53 Hz, 1H), 7.38-7.42 (m, 2H), 7.43-7.46 (m, 1H), 7.63-7.71 (m, 2H), 7.86 (s, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328107B2
出典データセットuspto-grants-2016_05
ORD IDord-1136de85f3c940d8ad92093b4336dc44
出典メモuspto-grants-2016_05