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HRID 1110191作成日:2026年10月26日

Tritylamine → Fmoc-Asn(Trt)-OH

https://huagongshe.com/reaction/1110191

反応式

関与物質

役割名称HCID仕込み量
反応物TritylamineHCID 138598—
反応物1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
反応物Fmoc-Asp-OBzlHCID 11224591—
溶媒1,2-DichloroethaneHCID 11—
溶媒Ethyl AcetateHCID 8857—
生成物Fmoc-Asn(Trt)-OHHCID 640248—

反応手順

0.8 ml of 1-chloro-N,N,2-trimethyl-prop-1-enylamine (A. Devos et al., J. Chem. Soc., Chem. Commun., Vol. 1979, p. 1180) is added to a stirred solution of 2.09 g of Fmoc-Asp-OBzl in 20 ml of 1,2-dichloroethane at 0° under an argon atmosphere. After 10 minutes, a solution of 1.2 g of tritylamine in 4 ml of 1,2-dichloroethane is added, and then the mixture is stirred for 2 hours, diluted with ethyl acetate and washed with water. The organic phase is dried and evaporated. The residue is taken up in chloroform and chromatographed on 250 g of silica gel. The fractions containing the Fmoc-Asn(Trt)-OBzl are combined and evaporated; the product is obtained as an amorphous foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05324833
出典データセットuspto-grants-1994_06
ORD IDord-77092f084bd54ee4913616dde60a2a08
出典メモuspto-grants-1994_06