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HRID 61597作成日:2026年10月25日

Diisopropylethylamine → 2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamide

https://huagongshe.com/reaction/61597

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Aminoacetonitrile sulfate (1:1)HCID 196971—
反応物PyBOPHCID 2724699—
反応物2-(3-(4-((1H-indazol-5-yl)amino)quinazolin-2-yl)phenoxy)acetic acidHCID 59361988—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-(3-(4-(1h-Indazol-5-ylamino)quinazolin-2-yl)phenoxy)-n-(cyanomethyl)acetamideHCID 11950521—

反応手順

A suspension of 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)acetic acid (70 mg, 0.14 mmol), PyBOP® (40 mg, 0.077 mmol), DIEA (24 μL, 0.14 mmol) in dry CH2Cl2:DMF (2:0.1 mL) was stirred at RT for 15 minutes. To this solution of activated acid was added aminoacetonitrile monosulfate (14 mg, 0.091 mmol). After 30 minutes, 1.0 equivalent of DIEA and 0.55 equivalents of PyBOP® were added. After stirring the solution for 15 minutes, 0.65 equivalents of aminoacetonitrile monosulfate were added and the mixture was stirred for an additional 30 minutes. The solvent was removed in vacuo and the crude product was purified using prep HPLC (15-40_90 mins) to afford 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(cyanomethyl)acetamide. (12 mg, 0.027 mmol, 19%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440961B2
出典データセットuspto-grants-2016_09
ORD IDord-f89e62fea6d8459780d59e2aaa880108
出典メモuspto-grants-2016_09