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HRID 1655682作成日:2026年10月26日

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

https://huagongshe.com/reaction/1655682

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US05250720
出典データセットuspto-grants-1993_10
ORD IDord-abe011cb3b3a40019232e414a44c4e89
出典メモuspto-grants-1993_10