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HRID 856007作成日:2026年10月24日

2-Methyl-1-butene → 4-(3-Phenylpyrazolo[1,5-a]pyrimidin-6-yl)benzoic acid

https://huagongshe.com/ja/reaction/856007

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-1-buteneHCID 11240—
反応物Sodium ChloriteHCID 23668197—
反応物Monosodium phosphateHCID 23672064—
反応物4-(3-Phenylpyrazolo[1,5-a]pyrimidin-6-yl)benzaldehydeHCID 58691600—
溶媒tert-ButanolHCID 6386—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-Phenylpyrazolo[1,5-a]pyrimidin-6-yl)benzoic acidHCID 58691610—

反応手順

A solution of 4-(3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)benzaldehyde (1-5, 250 mg, 0.835 mmol, 1 equiv) in a 4:1 mixture of THF and t-BuOH (20 mL) was treated with 2-methyl butene (5 mL), an aqueous solution of sodium phosphate monobasic (0.14 M, 230 mg, 1.67 mmol, 2 equiv) and sodium chlorite (194 mg, 2.15 mmol, 2.57 equiv). After 1 hour at 23° C., additional solid sodium phosphate monobasic (230 mg, 1.67 mmol, 2 equiv) and sodium chlorite (194 mg, 2.15 mmol, 2.57 equiv) were added. The reaction mixture was stirred for an additional 4 hours, concentrated, and the residue dissolved in EtOAc (100 mL) then washed with a 25:1 mixture of aqueous 10% sodium bisulfite solution and 10% potassium hydrogen sulfate solution (2×100 mL). The organic layer was dried over sodium sulfate and concentrated to afford 4-(3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)benzoic acid (3-1) as a yellow solid. LRMS m/z: Calc'd for C19H14N3O2 (M+H) 316.35, found 316.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262199B2
出典データセットuspto-grants-2007_08
ORD IDord-0b95bfcfe77846829e1ad4670325e0c6
出典メモuspto-grants-2007_08