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HRID 269640作成日:2026年10月25日

1,2-Dichloroethane → Benzyl {(1S)-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamate

https://huagongshe.com/reaction/269640

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Z-Ndelta-Boc-L-ornithineHCID 7350734—
反応物HCID 57440197HCID 57440197—
溶媒DimethylformamideHCID 6228—
生成物Benzyl {(1S)-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-[(tert-butoxycarbonyl)amino]butyl}carbamateHCID 86624497—

反応手順

Preparation takes place in analogy to Example 79A from 120 mg (0.33 mmol) of N5-(tert-butoxycarbonyl)-N2-[(benzyloxy)carbonyl]-L-ornithine and 136 mg (0.43 mmol) of tert-butyl{(4S)-5-amino-4-[(tert-butoxycarbonyl)amino]pentyl}carbamate (Example 86A) in 6 ml of dimethylformamide with the addition of 82 mg (0.43 mmol) of EDC and 13 mg (0.1 mmol) of HOBt. The product is purified by preparative RP-HPLC (mobile phase water/acetonitrile gradient: 90:10→5:95).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446102B2
出典データセットuspto-grants-2008_11
ORD IDord-6a5d5f563a0641039e4b732bbdf3c5f7
出典メモuspto-grants-2008_11