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HRID 473202作成日:2026年10月25日

Triphenyl phosphite → HCID 178488826、化合物

https://huagongshe.com/reaction/473202

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenyl phosphiteHCID 7540—
反応物2-Amino-3-methoxybenzoic acidHCID 255720—
反応物beta-Alanine, ethyl ester, hydrochlorideHCID 458475—
反応物2,2-Difluoro-2-(5-fluoropyridin-2-yl)acetic acidHCID 66609553—
溶媒PyridineHCID 1049—
生成物HCID 178488826HCID 17848882671%

反応条件

温度150 °C

反応手順

To 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetic acid from Example 33 step A (1 g, 5.23 mmol) and 2-amino-3-methoxybenzoic acid (875 mg, 5.23 mmol) in pyridine (15 mL) was added triphenyl phosphite (1.51 mL, 5.75 mmol) and the mixture was heated in a microwave synthesizer at 150° C. for 10 min. The mixture was allowed to cool to rt and then ethyl 3-aminopropanoate hydrochloride (883 mg, 5.75 mmol) was added. The mixture was heated in a microwave synthesizer at 190° C. for 4 min and then concentrated under reduced pressure. THF (10 mL) and sodium ethoxide (21% in EtOH, 4 mL) were added, and the mixture was stirred at 60° C. for 0.5 h. The mixture was allowed to cool and concentrated under reduced pressure. The residue was dissolved in water and the pH was adjusted to <4 by addition of 4 N HCl. The precipitate was collected by filtration, washed with water, and dried on the funnel to afford 2-(difluoro(5-fluoropyridin-2-yl)methyl)-8-methoxyquinazolin-4-ol (1.19 g, 71%). LC-MS (ESI) m/z 322 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633207B2
出典データセットuspto-grants-2014_01
ORD IDord-f15bdac829d74917a33560b0fcef7c35
出典メモuspto-grants-2014_01