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Triethylamine → 3-(4-Benzyloxy-phenyl)-2(S)-[(4-oxo-4H-chromene-3-carbonyl)-amino]-propionic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | Chromone-3-carboxylic acid | HCID 181620 | — |
| 反応物 | H-Tyr(Bzl)-OMe.HCl | HCID 12616037 | — |
| 触媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(4-Benzyloxy-phenyl)-2(S)-[(4-oxo-4H-chromene-3-carbonyl)-amino]-propionic acid methyl ester | HCID 53956822 | 9.1% |
反応手順
To a stirring solution of 360 mg (2 mmol) of chromone-3-carboxylic acid in 25 mL of CH2Cl2 at 0° C. were added several drops of DMF followed by 1 mL of 2M solution of oxalyl chloride in CH2Cl2. The resulting solution was stirred 3 h at rt and 643 mg (2 mmol) of O-benzyl-L-tyrosine methyl ester hydrochloride and 0.2 g (2.0 mmol) of triethylamine in 15 mL of CH2Cl2 were added and stirring continued overnight. Solvent was removed under reduced pressure. Product was purified by LCC on SiO2 (Hexane: EtOAc 13:7) providing 83 mg of title compound as a white solid: low resolution MS (ES+ (M+H), 458; RP-HPLC (Dynamax C-8 25 cm×4.1 mm; 50-90% CH3CN in H2O with 0.1% TFA buffer; 15 minutes; 2 mL/min): tr=10.44 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06294580B1 |
| 出典データセット | uspto-grants-2001_09 |
| ORD ID | ord-e12dc4bff32f48e4a04f8479379b085c |
| 出典メモ | uspto-grants-2001_09 |