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HRID 1392298作成日:2026年10月27日

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

https://huagongshe.com/reaction/1392298

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US07342037B2
出典データセットuspto-grants-2008_03
ORD IDord-6e188fdea4f941178a5553e35ab5ee9f
出典メモuspto-grants-2008_03