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L-Alanine → N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | L-Alanine | HCID 5950 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Boc-Ala-OSu | HCID 11011585 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine | HCID 6992569 | — |
反応手順
L-Alanine (3.57 g, 40 mmol) was dissolved in 18.8 ml of Triton B (40 mmol), evaporated to dryness, and the oily residue re-evaporated twice with DMF (30 ml each). The salt obtained was stirred with 11.45 g of Boc-Ala-OSu (40 mmol) in 40 ml DMF, with 4 ml of NMM added, for 20 hours. The solvent was removed and the residue taken up in 10% HOAc (100 ml). The product was extracted into EtOAc (4 times 100 ml), washed twice with a small volume of H2O, dried over Na2SO4, evaporated to a small volume, and treated with petroleum ether until cloudiness developed. A crystalline product formed on storage in the refrigerator overnight: Yield, 8.2 g (76.3%); mp 115°-118°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04148788 |
| 出典データセット | uspto-grants-1979_04 |
| ORD ID | ord-9889250ba2dc449bb2d7d2a9635c9889 |
| 出典メモ | uspto-grants-1979_04 |