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HRID 16945作成日:2026年10月25日

alpha-Naphthyl isocyanate → 1-(3-Tert-butyl-1-(3-(2-morpholino-2-oxoethyl)phenyl)-1h-pyrazol-5-yl)-3-(naphthalen-1-yl)urea

https://huagongshe.com/reaction/16945

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-(3-t-butyl-5-amino-1H-pyrazol-1-yl)phenyl]-1-morpholinoethanoneHCID 21867345—
溶媒DichloromethaneHCID 6344—
生成物1-(3-Tert-butyl-1-(3-(2-morpholino-2-oxoethyl)phenyl)-1h-pyrazol-5-yl)-3-(naphthalen-1-yl)ureaHCID 21867339—

反応手順

A mixture of Example L (0.2 g, 0.58 mmol) and 1-naphthylisocyanate (0.10 g, 0.6 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 purified by column chromatography using ethyl acetate/hexane/CH2Cl2 (3/1/0.7) as the eluent (0.11 g, off-white solid) to yield 1-{3-tert-butyl-1-[3-(2-morpholino-2-oxoethyl)phenyl]-1H-pyrazol-5-yl}-3-(naphthalene-1-yl)urea. mp: 194-196; 1H NMR (200 MHz, DMSO-d6): δ 9.07 (1H, s), 8.45 (s, 1H), 8.06-7.93 (m, 3H), 7.69-7.44 (m, 7H), 7.33-7.29 (d, 6.9 Hz, 1H), 6.44 (s, 1H), 3.85 (m, 2H), 3.54-3.45 (m, 8H), 1.31 (s, 9H); MS:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737283B2
出典データセットuspto-grants-2010_06
ORD IDord-3d6c2a70a5244194aac4fd5b3b2d9622
出典メモuspto-grants-2010_06