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2-Amino-5-chlorobenzoic acid → (R)-1-(4-chlorobenzyl)-3-[[N-(2-amino-5-chlorobenzoyl)glycyl]amino]pyrrolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-5-chlorobenzoic acid | HCID 12476 | — |
| 反応物 | Diisopropylcarbodiimide | HCID 12734 | — |
| 反応物 | (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine | HCID 54551710 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | (R)-1-(4-chlorobenzyl)-3-[[N-(2-amino-5-chlorobenzoyl)glycyl]amino]pyrrolidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07390830B1 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-051527a456854e87ace95143e4d333ed |
| 出典メモ | uspto-grants-2008_06 |