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HRID 2098810作成日:2026年10月25日

Triethylamine → N-((2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-2-(dimethylamino)acetamide

https://huagongshe.com/reaction/2098810

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Glycine, N,N-dimethyl-, ethyl esterHCID 118412—
反応物(2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanamineHCID 46180727—
溶媒DichloromethaneHCID 6344—
生成物N-((2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-2-(dimethylamino)acetamideHCID 86618441—

反応手順

To a solution of (2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanamine 27 from Example 11 (50 mg, 0.2 mmol) in CH2Cl2 (4 mL) was added Et3N (84 μL, 0.6 mmol) and dimethylglycine ethyl ester (0.3 mmol). The reaction stirred 18-48 h at room temperature before being quenched with water. The aqueous layer was extracted with EtOAc. The combined organics were dried over Na2SO4 and concentrated in vacuo to give N-((2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-2-(dimethylamino)acetamide which was utilized in a Suzuki coupling according to General Procedure A. The crude material was purified by reversed phase HPLC to give 350 (10 mg). MS (Q1) 452 (M)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08450315B2
出典データセットuspto-grants-2013_05
ORD IDord-d0c41762a79f4076903201e811f9894b
出典メモuspto-grants-2013_05