関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | Sulfuric acid methanol | HCID 18363649 | — |
| 反応物 | Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoate | HCID 86711343 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl 2-(5-iodo-3,4-dihydroisoquinolin-1-yl)propanoate | HCID 86711344 | 12.2% |
反応手順
A solution of methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoate (9.9 g, 27.4 mmol) in DCM (120 mL) was treated with oxalyl chloride (2.59 mL, 30.2 mmol) and the mixture was stirred at RT for 30 min. FeCl3 (5.34 g, 32.9 mmol) was then added portionwise at 0° C. and the resulting brown mixture was stirred at RT for 4 h. A 2N aqueous solution of HCl (35 mL) was then added and the mixture was stirred at RT for another 2 h. The mixture was then diluted with H2O and extracted with DCM. The combined org. phases were then dried over Na2SO4, filtered and concentrated in vacuo. The brown residue obtained was taken up in a 19:1 mixture of MeOH/H2SO4 (120 mL) and stirred at reflux for 3 h. The mixture was then concentrated in vacuo and the brown reside obtained was taken up in H2O. The mixture was rendered basic with ammonia and then extracted with AcOEt. The combined org. phases were dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (SiO2, cHex/AcOEt 100:0 to 70:30) gave the title compound (1.15 g) as yellow oil. UPLC-MS: MS 344.1 (M+H+); UPLC rt 0.96 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08853203B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-0ca03d1b97484d15b3676085b7b7a6ac |
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| 出典メモ | uspto-grants-2014_10 |
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