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HRID 964491作成日:2026年10月26日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Cbz-Asp(OBut)-Gly-OBn

https://huagongshe.com/reaction/964491

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartateHCID 111082—
反応物Benzyl 2-aminoacetate hydrochlorideHCID 11701227—
溶媒DichloromethaneHCID 6344—
溶媒ChlorineHCID 24526—
生成物Cbz-Asp(OBut)-Gly-OBnHCID 14375963108.9%

反応手順

A mixture of Cbz-Asp(OBut)-OH (3590 mg, 11.1 mmol), HCl+H-Gly-OBn (3360 mg, 16.6 mmol), EDCI (3180 mg, 16.6 mmol), HOBt (2250 mg, 16.6 mmol) and DIEA (2900 mg, 16.6 mmol) in dry CH2 Cl2 (50 mL) was stirred at r.t. for six hours. The reaction mixture was added CH2Cl2 (150 mL) and washed with 1N HCl (200 mL), saturated NaHCO3 aq. (200 mL) and brine (200 mL). The organic layer was passed through an inch of SiO2 layer and the SiO2 was washed with 1/9=AcOEt/CH2Cl2 (200 mL). The eluent was evaporated in vacuo to give clear oil (5690 mg, 100%): 1H NMR (300 MHz, CDCl3) δ 7.368 (s, 10H), 7.082 (t, 1H), 6.013 (d, J=7.8 Hz, 1H), 5.164 (s, 2H), 5.126 (s, 2H), 4.592 (d, J=6.6 Hz, 1H), 4.072 (d, J=5.7 Hz, 2H), 2.891 (dd, J=18.2, 4.5 Hz, 1H), 2.641 (dd, J=17.1, 6.3 Hz, 1H), 1.423 (s, 9H); 13C NMR (300 MHz, CDCl3) δ 171.0, 170.9, 169.3, 136.1, 135.2, 129.7, 128.6 (2C), 128.4, 128.3, 128.2, 81.9, 67.3, 67.2, 51.1, 41.5, 37.3, 28.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05770380
出典データセットuspto-grants-1998_06
ORD IDord-874846bbe82a4e449dc38c8d22cfa6f1
出典メモuspto-grants-1998_06