関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Acetyl-D-Mannosamine | HCID 439281 | — |
| 反応物 | 3-Butenoic acid, ion(1-) | HCID 6971089 | — |
| 反応物 | Ethylacetate methanol | HCID 21584119 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | GlyTouCan:G94857MO | HCID 14160859 | 92% |
反応手順
In 2 mL of DMF were suspended 500 mg (2.2 mmol) of N-acetylmannosamine. Vinylacetate (1 mL, 5 equivalent) and 160 mg of subtilisin mutant 8399 [Zhong et al., J. Am. Chem. Soc., 113:683 (1991)] were then added and the suspension was stirred vigorously at room temperature. The reaction progress was monitored by TLC with ethyl acetate/methanol (2/1). After 5 hours when the formation of the di-acetylated derivatives began, the reaction was stopped by evaporating the vinylacetate and DMF. Methanol was then added to dissolve the sugar. After the enzyme and salt were filtered off, the filtrate was concentrated. The residual syrup was chromatographed on a silica gel, with ethyl acetate/methanol (10/1) to give 6-O-Acetyl N-acetylmannosamine (92 percent) as α/β mixture (3:1) based on the NMR spectrum.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06168934A |
|---|
| 出典データセット | uspto-grants-2001_01 |
|---|
| ORD ID | ord-e48bf7cb11cf462f8684c6dcf134cf78 |
|---|
| 出典メモ | uspto-grants-2001_01 |
|---|