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HRID 1804465作成日:2026年10月26日

Dimethyl nitromalonate → Methyl 4-cyclopropyl-5-phenylisoxazole-3-carboxylate

https://huagongshe.com/reaction/1804465

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl nitromalonateHCID 226085—
反応物(Cyclopropylethynyl)benzeneHCID 10888024—
溶媒MesityleneHCID 7947—
生成物Methyl 4-cyclopropyl-5-phenylisoxazole-3-carboxylateHCID 58537215—

反応手順

A solution of (cyclopropylethynyl)benzene (300 mg, 2.110 mmol) and dimethyl nitromalonate (0.854 mL, 6.33 mmol) in mesitylene (4 mL) was heated to 150° C. for 16 h. The reaction mixture was concentrated to yield a crude product which was purified by silica gel chromatography with hexanes/ethyl acetate (10/1) to yield methyl 4-cyclopropyl-5-phenylisoxazole-3-carboxylate. The compound was re-purified by preparative HPLC [Column: PHENOMENEX® S10 30×100 mm; Gradient time: 10 min; Flow rate=40 ml/min; Solvent A=10% MeOH−90% Water−0.1% TFA; Solvent B=90% MeOH−10% water−0.1% TFA; Start % B=20; Final % B=100] to yield methyl 4-cyclopropyl-5-phenylisoxazole-3-carboxylate (170 mg). The compound had an HPLC ret. time=2.77 min.−Column. YMC S5 COMBISCREEN® 4.6×50 mm; Gradient time: 4 min; Flow rate=4 ml/min; Solvent A=10% MeOH−90% Water−0.2% H3PO4; Solvent B=90% MeOH−10% water−0.2% H3PO4; Start % B=0; Final % B=100. LC-MS: M+1=244+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08354398B2
出典データセットuspto-grants-2013_01
ORD IDord-14c5b1ff1de04fc18edcaea083ae3854
出典メモuspto-grants-2013_01