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HRID 549796作成日:2026年10月25日

5-Amino-7-chloro-3-(2,3,5'-tri-O-acetyl-beta-D-ribofuranosyl)-thiazolo[4,5-d]pyrimidin-2-one → 5-Amino-3-(2',3,5'-tri-O-acetyl-beta-D-ribofuranosyl)-3H-thiazolo[4,5-d]pyrimidin-2-one

https://huagongshe.com/reaction/549796

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-7-chloro-3-(2,3,5'-tri-O-acetyl-beta-D-ribofuranosyl)-thiazolo[4,5-d]pyrimidin-2-oneHCID 59533920—
溶媒Acetic AcidHCID 176—
生成物5-Amino-3-(2',3,5'-tri-O-acetyl-beta-D-ribofuranosyl)-3H-thiazolo[4,5-d]pyrimidin-2-oneHCID 1163326790%

反応手順

A flame-dried round bottom flask was charged with 80 (4.37 g, 9.48 mmol) and glacial acetic acid (61 mL). The flask was sealed with a septum and flushed with nitrogen. Zinc-copper couple (6.07 g, Aldrich) was added and the reaction stirred at room temperature for a period of 21 h. The reaction was then heated to 80° C. for 1 h. The reaction mixture was cooled to room temperature, filtered thru a pad of Celite®, washed with EtOAc (200 mL) and concentrated under vacuum. The resulting white solid (residue) was diluted with CH2Cl2 (250 mL) and washed with 0.5 M NaOH (500 mL). The aqueous layer was extracted with CH2Cl2 (2×150 mL) and the combined organic layers were dried (MgSO4), filtered and concentrated. Purification by flash chromatography (SiO2, 5% Acetone-CH2Cl2) afforded 78 (3.64 g, 90%) as a white powder identical in all respects to material isolated in Example 38, step 2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943759B2
出典データセットuspto-grants-2011_05
ORD IDord-bd40428ec63641fab9f8e4bb0043c82f
出典メモuspto-grants-2011_05