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Succinic anhydride → 4-(5-Bromo-2-thienyl)-4-oxobutyric acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Succinic anhydride | HCID 7922 | — |
| 反応物 | 2-Bromothiophene | HCID 13851 | — |
| 生成物 | 4-(5-Bromo-2-thienyl)-4-oxobutyric acid | HCID 11184604 | 51% |
反応手順
As described for Example 1, 0.3 mole of 2-bromothiophene is reacted with succinic anhydride to give 4-(5-bromo-2-thienyl)-4-ketobutyric acid (51%), m.p. 141°-143° C. The preceding compound is coupled to L-proline to give 1-[3-(5-bromo-2-thenoyl)propionyl]-L-proline (56%) as crystals, m.p. 166°-168° C. The preceding compound (0.008 mole) is reacted with bromine in acetic acid to yield 1-[3-bromo-3-(5-bromo-2-thenoyl)propionyl]-L-proline as a glass (97%). As for Example 1, reaction of the preceding compound with sodium thioacetate gives the product of the Example (88%) as a yellow glass.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04342691 |
| 出典データセット | uspto-grants-1982_08 |
| ORD ID | ord-36e951190a654ea481d3cb8aebdc008f |
| 出典メモ | uspto-grants-1982_08 |