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HRID 279282作成日:2026年10月27日

Diisopropylcarbodiimide → 3-[[N-(2-amino-4,5-difluorobenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)pyrrolidine

https://huagongshe.com/reaction/279282

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-Amino-4,5-difluorobenzoic acidHCID 735965—
反応物1-(4-Chlorobenzyl)-3-[(glycylamino)methyl]pyrrolidineHCID 18426257—
溶媒ChloroformHCID 6212—
溶媒tert-ButanolHCID 6386—
生成物3-[[N-(2-amino-4,5-difluorobenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)pyrrolidineHCID 508849—

反応手順

A solution of 1-(4-chlorobenzyl)-3-{(glycylamino)methyl}pyrrolidine (0.050 mmol) in CHCl3 (1.35 mL) and tert-butanol (0.05 mL) was treated with 2-amino-4,5-difluorobenzoic acid (0.060 mmol), diisopropylcarbodiimide (0.060 mmol), and HOBt (0.060 mmol). The reaction mixture was stirred at room temperature for 19 h. The mixture was loaded onto Varian™ SCX column, and washed with CH3OH/CHCl3 1:1 (10 mL) and CH3OH (10 mL). Product was eluted off using 2 N NH3 in CH3OH (5 mL) and concentrated to afford 3-[{N-(2-amino-4,5-difluorobenzoyl)glycyl}aminomethyl]-1-(4-chlorobenzyl)pyrrolidine (Compound No. 1506) (22.0 mg, quant): The purity was determined by RPLC/MS (92%); ESI/MS m/e 437 (C21H23ClF2N4O2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362177B1
出典データセットuspto-grants-2002_03
ORD IDord-97d2064fc8cf446c8609e0045adfca72
出典メモuspto-grants-2002_03