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HRID 525087作成日:2026年10月25日

Formamide → HCID 178422246、化合物

https://huagongshe.com/reaction/525087

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物Ethyl 2-Amino-5-methylthiophene-3-carboxylateHCID 4062885—
生成物HCID 178422246HCID 17842224625%

反応手順

Into a 25-mL round-bottom flask placed ethyl 2-amino-5-methylthiophene-3-carboxylate (500 mg, 2.70 mmol, 1.00 equiv) in 10 mL of formamide was stirred for 8 h at 180° C. in an oil bath. After completion of the reaction, the reaction mixture was cooled down to room temperature and then quenched with water/ice, extracted with 3×50 mL of ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified on a silica gel column with ethyl acetate/petroleum ether (2:1) to provide the resulted 6-methylthieno[2,3-d]pyrimidin-4-ol (114 mg, 25%) as a yellow solid. MS (ES, m/z): 167 [M+H+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340554B2
出典データセットuspto-grants-2016_05
ORD IDord-930bafd7c22541e49b7e9d609d7c21c1
出典メモuspto-grants-2016_05