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HRID 221478作成日:2026年10月25日

Methyl chloroacetate → 7-tert-Butyl 1-methyl 3-(trifluoromethyl)-5H,6H,7H,8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylate

https://huagongshe.com/reaction/221478

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroacetateHCID 7295—
反応物Potassium CarbonateHCID 11430—
反応物tert-butyl 1-bromo-3-(trifluoromethyl)-5H,6H,7H,8H-imidazo(1,5-a)pyrazine-7-carboxylateHCID 57518451—
触媒Dicobalt Octacarbonyl (stabilized with 1-5% Hexane)HCID 25049—
溶媒MethanolHCID 887—
生成物7-tert-Butyl 1-methyl 3-(trifluoromethyl)-5H,6H,7H,8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylateHCID 5751845267.8%

反応手順

Octacarbonyldicobalt (5.54 g, 16.2 mmol) and potassium carbonate (11.2 g, 81.1 mmol) was dissolved in 100 mL of methanol under stirring. The reaction mixture was stirred for 15 minutes at 60° C., and 1-bromo-3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazine-7-carboxylic acid tert-butyl ester 27b (3 g, 8.11 mmol) and methyl chloroacetate (5.25 g, 48.6 mmol) were then added to the solution. The reaction mixture was reacted for 6 hours under a carbon monoxide atmosphere and monitored by thin layer chromatography until the disappearance of the starting materials. After cooling to room temperature, the reaction mixture was filtered through a pad of silica gel, rinsed with methanol. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 3-trifluoromethyl-5,6-dihydro-8H-imidazo[1,5-a]pyrazine-1,7-dicarboxylic acid 7-tert-butyl ester 1-methyl ester 27c (1.92 g, yield 67%) as a white solid. (Reference: J. Organomet. Chem, 1985, 293)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207161B2
出典データセットuspto-grants-2012_06
ORD IDord-d14ccd8083c348e4b44b3ecc9a3d721c
出典メモuspto-grants-2012_06