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HRID 2249526作成日:2026年10月27日

Triethylamine → 4-(2,3-Difluoro-benzoylamino)-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2249526

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,3-Difluorobenzoyl chlorideHCID 519549—
反応物4-Amino-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 59639716—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2,3-Difluoro-benzoylamino)-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 6928743281.2%

反応手順

To a solution of 4-amino-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid ethyl ester (1 g, 4.3 mmol) and triethylamine (650 mg, 6.4 mmol) in dry CH2Cl2 (20 mL) was added 2,3-difluoro-benzoyl chloride (760 mg, 4.3 mmol). The mixture was stirred at RT for 3 h and diluted with EtOAc (150 mL). After washing with 2N HCl (80 mL) and NaHCO3 (2×80 mL), the organic layer was dried over MgSO4, filtered, and evaporated to give a yellow solid (1.3 g, 81%). This solid was dried on the vacuum pump for 14 hrs and then was used for the next step directly. MS (ES+): m/e=373.2 (M+H); LC: 3.45 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07314885B2
出典データセットuspto-grants-2008_01
ORD IDord-a2a8d47a122e43349ba57717c69b9894
出典メモuspto-grants-2008_01