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HRID 133558作成日:2026年10月25日

2-Amino-5-chlorobenzoic acid → (R)-1-(4-chlorobenzyl)-3-[[N-(2-amino-5-chlorobenzoyl)glycyl]amino]pyrrolidine

https://huagongshe.com/reaction/133558

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-5-chlorobenzoic acidHCID 12476—
反応物DiisopropylcarbodiimideHCID 12734—
反応物(R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidineHCID 54551710—
溶媒ChloroformHCID 6212—
生成物(R)-1-(4-chlorobenzyl)-3-[[N-(2-amino-5-chlorobenzoyl)glycyl]amino]pyrrolidineHCID 44453533—

反応手順

2-Amino-5-chlorobenzoic acid (0.060 mL) and diisopropylcarbodiimide (0.060 mol) were added to a chloroform (2 mL) solution of (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine (0.050 mmol). The resulting reaction solution was stirred at room temperature for 15 hours. The mixture solution was loaded onto a Varian™ SCX column and washed with methanol (15 mL). The obtained crude product was eluted with a solution of 2 M NH3 in methanol (5 mL) and concentrated to thereby afford (R)-1-(4-chlorobenzyl)-3-[N-[2-amino-5-chlorobenzoyl]glycyl]amino]pyrrolidine (Compd. No. 1084) (12.7 mg, 60%). The purity was determined by RPLC/MS (87%). ESI/MS m/e 421.0 (M++H, C20H22Cl2N4O2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390830B1
出典データセットuspto-grants-2008_06
ORD IDord-051527a456854e87ace95143e4d333ed
出典メモuspto-grants-2008_06