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HRID 443922作成日:2026年10月26日

Ethylmorpholine → Boc-MePhe methioninol

https://huagongshe.com/reaction/443922

反応式

関与物質

役割名称HCID仕込み量
反応物EthylmorpholineHCID 7525—
反応物Isobutyl chloroformateHCID 62365—
反応物L-MethioninolHCID 2724404—
反応物Boc-N-Me-Phe-OHHCID 7010602—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物Boc-MePhe methioninolHCID 131712176—

反応手順

3.1 g of Boc-MePhe-OH are dissolved in 30 ml of tetrahydrofuran, cooled to -20°, and 1.45 ml of N-ethylmorpholine are added with stirring followed by 1.45 ml of chloroformic acid iso-butyl ester and the mixture stirred for a further 5 minutes at -20°. A cold solution of 1.80 g of methioninol in 1 ml of tetrahydrofuran is added, the mixture left to stand for 2 hours at a temperature of from -5° to 0° and then stirred for 2 hours at room temperature. The reaction mixture is diluted with ca. 350 ml of acetic acid and washed repeatedly with water, 1 N citric acid, 10% KHCO3 and 30% NaCl solution. The organic phase is dried over Na2SO4 and evaporated, whereby Boc-MePhe-methioninol is obtained as an amorphous product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04261888
出典データセットuspto-grants-1981_04
ORD IDord-a177efbe882b49f99b0a5f2d55b737f4
出典メモuspto-grants-1981_04