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HRID 842735作成日:2026年10月25日

5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl Ester → 5-(3-tert-Butoxycarbonylamino-propyl)-thiophene-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/842735

反応式

関与物質

役割名称HCID仕込み量
反応物5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 54075339—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物5-(3-tert-Butoxycarbonylamino-propyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 5413889792.4%

反応手順

A solution of 5-(3-tert-butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic acid methyl ester (2.06 g) and 10% Pd/C (1.03 g) in 50 mL MeOH was placed in a Parr shaker and was hydrogenated at 50 psi H2 for 16 h. The reaction was filtered through Celite® with the aid of MeOH and the filtrate was concentrated in vacuo to afford the title compound of Step B as a solid (1.93 g). MS 317 (M+18).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06376502B1
出典データセットuspto-grants-2002_04
ORD IDord-cc74a04dcac44b309f8fa6c3efd40b93
出典メモuspto-grants-2002_04