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HRID 254761作成日:2026年10月25日

Acetic Acid → (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine

https://huagongshe.com/reaction/254761

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2-Amino-5-bromopyrazineHCID 599539—
反応物1,3-dimethyl-1H-pyrazole-4-carbaldehydeHCID 847285—
反応物Borane,N-dimethylmethanamine (1:1)HCID 6327651—
溶媒Ethyl AcetateHCID 8857—
生成物(5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amineHCID 8661430392.9%

反応手順

A mixture of 1,3-dimethyl-1H-pyrazole-4-carbaldehyde (142 mg, 1.145 mmol), 2-amino-5-bromopyrazine (200 mg, 1.149 mmol), borane trimethylamine complex (126 mg, 1.73 mmol) and glacial acetic acid (137 mg, 2.29 mmol) in anhydrous methonol (3 ml) was stirred at room temperature overnight. The reaction mixture was then diluted with ethyl acetate, washed with water, dried over MgSO4 and filtered. The filtrate was concentrated to give 300 mg of (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine as crude product, which was used for next step reaction without further purification. Crude yield: 93%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07875622B2
出典データセットuspto-grants-2011_01
ORD IDord-38087498dc564989a3268c1e6140769d
出典メモuspto-grants-2011_01