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Dicyclohexylcarbodiimide → Benzyl N-[(1S)-1-(methylcarbamoyl)-2-phenylethyl]carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Benzyloxycarbonyl-L-phenylalanine | HCID 70878 | — |
| 反応物 | N-Hydroxysuccinimide | HCID 80170 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Benzyl N-[(1S)-1-(methylcarbamoyl)-2-phenylethyl]carbamate | HCID 13443905 | 107.3% |
反応手順
A mixture of 1.00 g of Cbz-Phe-OH (Sigma Chemical Company), 0.385 g of N-hydroxysuccinimide and 0.541 g of 1,3-dicyclohexylcarbodiimide in 5 mL of dry THF was kept at 4° C. under N2 overnight. The resulting precipitate was removed by filtration, and to the filtrate was added excess 40% aqueous methylamine at room temperature. The mixture was stirred at room temperature for 30 min. The solid was removed by filtration and the filtrate was partitioned between saturated aqueous NaHCO3 and CH2Cl2. The organic layer was separated, dried over anhydrous Na2SO4, and evaporated under reduced pressure to give 1.12 g of the crude Cbz-Phe-NHMe.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05470834 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-a1374cc68e8a4265af61199157d2232f |
| 出典メモ | uspto-grants-1995_11 |