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HRID 491998作成日:2026年10月24日

1-Naphthoyl fluoride → HCID 58842868、化合物

https://huagongshe.com/ja/reaction/491998

反応式

関与物質

役割名称HCID仕込み量
反応物1-Naphthoyl fluorideHCID 263223—
反応物ethyl 3-(3-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl)propanoateHCID 58842892—
溶媒DichloromethaneHCID 6344—
生成物HCID 58842868HCID 58842868372.7%

反応手順

A solution of Example Z (315 mg, 1.0 mmol) and Barton's base (0.5 mL) in anhydrous CH2Cl2 (5 mL) under N2 was stirred at RT for 30 min, and then added to a solution of naphthalene-1-carbonyl fluoride (348 mg, 0.2 mmol) in anhydrous CH2Cl2 (5 mL). The resulting mixture was stirred at RT overnight. After quenching with water (100 mL), the reaction mixture was extracted with ethyl acetate (3×100 mL). The combined organic extracts were washed with brine, dried (NaSO4), filtered and concentrated under reduced pressure to yield a residue which was purified by flash chromatography to afford 3-(3-{3-t-butyl-5-[(naphthalene-1-carbonyl)-amino]-pyrazol-1-yl}-phenyl)-propionic acid ethyl ester, (350 mg, 74%). 1H-NMR (CDCL3): 8.29 (d, J=8.0 Hz, 1H), 7.98 (d, J=7.2 Hz, 2H), 7.89 (d, J=7.2 Hz, 1H), 7.62-7.57 (m, 3H), 7.49-7.28 (m, 4H), 7.03 (s, 1H), 3.94 (q, J=7.2 Hz, 2H), 2.96 (t, J=7.2 Hz, 2H), 2.58 (t, J=7.2 Hz, 2H), 1.45 (s, 9H), 1.13 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 470 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531566B2
出典データセットuspto-grants-2009_05
ORD IDord-11924aac28104479988971c8ef9d4840
出典メモuspto-grants-2009_05