反应详情

In 80 ml of H2O was suspended 4.50 g of H-Asn-OH.H2O, followed by addition of 80 ml of a THF solution containing 4.20 ml of triethylamine and 14.13 g of Boc-Ser(Bzl)-OSu under ice-cooling. The mixture was stirred at room temperature for 20 hours, after which the THF was distilled off. The residual aqueous solution was adjusted to pH 3 with 1M citric acid under ice-cooling and the resulting oily product was extracted with 200 ml of ethyl acetate. The extract was washed with 50 ml of saturated aqueous sodium chloride solution twice, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was treated with ether/petroleum ether (2:1) for solidification and the resultant powder was reprecipitated from methanol-isopropyl ether to give 8.74 g of Boc-Ser(Bzl)-Asn-OH (yield 71.2%). mp: 138°-139° C. [α]D22 : 10.2° (c=1, DMF) Rf: 0.54 (chloroform:methanol:acetic acid=7:2:1) Amino acid analysis: Asp 1.14 (1), Ser 0.86 (1)

1. temperaturecooling
2. distillationafter which the THF was distilled off
3. temperaturecooling
4. extractionthe resulting oily product was extracted with 200 ml of ethyl acetate
5. washThe extract was washed with 50 ml of saturated aqueous sodium chloride solution twice
6. dry with materialdried over anhydrous sodium sulfate
7. concentrationconcentrated under reduced pressure
8. additionThe residue was treated with ether/petroleum ether (2:1) for solidification
9. customthe resultant powder was reprecipitated from methanol-isopropyl ether