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HRID 454083作成日:2026年10月25日

Triphenylphosphine → 4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline

https://huagongshe.com/reaction/454083

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物1-PyrrolidinepropanolHCID 209342—
反応物7-Hydroxy-4-(2-methylindol-5-yloxy)quinazolineHCID 135763114—
溶媒DichloromethaneHCID 6344—
生成物4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazolineHCID 2203082335.8%

反応手順

Diisopropyl azodicarboxylate (146 mg, 0.72 mmol) was added to a solution of 7-hydroxy-4-(2-methylindol-5-yloxy)quinazoline (100 mg, 0.34 mmol), triphenyl phosphine (189 mg, 0.72 mol), and 3-pyrrolidinopropan-1-ol (89 mg, 0.686 mmol), (J. Org. Chem. 1988, 53, 3164), in methylene chloride (2.5 ml). After stirring overnight at ambient temperature, the solid was filtered. The filtrate was purified by column chromatography eluting with ethyl acetate/methylene chloride (1/1) followed by ethyl acetate/methylene chloride/methanol (4/5/1), methylene chloride/methanol (9/1) and 3N ammonia in methanol/methylene chloride (1/9). After removal of the solvent, the residue was triturated with ether, filtered, and dried under vacuum to give 4-(2-methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline (49 mg, 35%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492560B2
出典データセットuspto-grants-2013_07
ORD IDord-e98edf82ec354b419fca0bd04427b408
出典メモuspto-grants-2013_07