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HRID 4983作成日:2026年10月23日

N-(tert-butoxycarbonyl)glycine → Boc-Gly-Leu-Ala-OBzl

https://huagongshe.com/ja/reaction/4983

反応式

関与物質

役割名称HCID仕込み量
反応物N-(tert-butoxycarbonyl)glycineHCID 78288—
反応物H-Leu-Ala-OBzlHCID 16742166—
生成物Boc-Gly-Leu-Ala-OBzlHCID 131717744—

反応手順

Boc-Gly-Leu-Ala-OBzl was prepared by coupling Boc-Gly-OH (5.70 g, 32.6 mmoles) to H-Leu-Ala-OBzl using the mixed anhydride procedure described in Example 2. The product (13.8 g) was obtained as an amorphous solid. Boc-Gly-Leu-Ala-OBzl was deblocked with trifluoroacetic acid by the procedure described for the preparation of H-Leu-Ala-OBzl except that the trifluoroacetate salt was soluble in ether. The preparation was dissolved in ethyl acetate and treated with anhydrous hydrogen chloride. The resulting product was precipitated by the addition of ether to yield 7.7 g of H-Gly-Leu-Ala-OBzl HCl in a first crop.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242904
出典データセットuspto-grants-1993_09
ORD IDord-e95bb68602144d5c8b548570c446fb1d
出典メモuspto-grants-1993_09