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HRID 491985作成日:2026年10月24日

alpha-Naphthyl isocyanate → 2-(3-(3-tert-butyl-5-(3-naphthalen-1-ylureido)-1H-pyrazol-1-yl)phenyl)acetamide

https://huagongshe.com/ja/reaction/491985

反応式

関与物質

役割名称HCID仕込み量
反応物alpha-Naphthyl isocyanateHCID 66589—
反応物2-(3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenyl)acetamideHCID 21867307—
溶媒DichloromethaneHCID 6344—
生成物2-(3-(3-tert-butyl-5-(3-naphthalen-1-ylureido)-1H-pyrazol-1-yl)phenyl)acetamideHCID 2186731068.3%

反応手順

A mixture of Example N (2 g, 0.73 mmol) and 1-naphthylisocyanate (0.124 g, 0.73 mmol) in dry CH2Cl2 (4 ml) was stirred at RT under N2 for 18 h. The solvent was removed in vacuo and the crude product was washed with ethyl acetate (8 ml) and dried in vacuo to yield 1-{3-tert-butyl-1-[3-(carbamoylmethyl)phenyl)-1H-pyrazol-5-yl}-3-(naphthalene-1-yl)urea as a white solid (0.22 g). mp: 230 (dec.); 1H NMR (200 MHz, DMSO-d6): δ 9.12 (s, 1H), 8.92 (s, 1H), 8.32-8.08 (m, 3H), 7.94-7.44 (m, 8H), 6.44 (s, 1H), 3.51 (s, 2H), 1.31 (s, 9H); MS:

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-7c0a7be5a9f64f0aae57db01a54437ec
出典メモuspto-grants-2009_05