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HRID 1355734作成日:2026年10月27日

Benzyl Alcohol → 2-Amino-4-benzyloxy-6-furan-2-yl-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1355734

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物2-Amino-4-furan-2-yl-6-methanesulfonyl-pyrimidine-5-carbonitrileHCID 18507399—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Amino-4-benzyloxy-6-furan-2-yl-pyrimidine-5-carbonitrileHCID 981458156%

反応条件

温度100 °C

反応手順

To a stirred suspension of 300 mg (1.14 mmol) 2-amino-4-furan-2-yl-6-methanesulfonyl-pyrimidine-5-carbonitrile in 9 ml dimethoxyethane were added 0.41 ml (4.0 mmol) benzyl alcohol and 0.25 ml (1.7 mmol) DBU and the mixture heated at 100° C. for 1 hour. The reaction mixture was then concentrated in vacuo. Chromatography (ethyl acetate/hexane 2/1) followed by trituration in ether/hexane afforded 185 mg (56%) 2-amino-4-benzyloxy-6-furan-2-yl-pyrimidine-5-carbonitrile as a white crystalline solid. EI-MS m/e (%): 292 (M+, 40), 91 (C7H7+, 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06586441B2
出典データセットuspto-grants-2003_07
ORD IDord-43fd914ddf3e4ff29c59ab53cf3367e3
出典メモuspto-grants-2003_07