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HRID 381692作成日:2026年10月27日

Methanethiol → 2'-Deoxy-2'-methylthio-5-methyluridine

https://huagongshe.com/reaction/381692

反応式

関与物質

役割名称HCID仕込み量
反応物MethanethiolHCID 878—
反応物1,1,3,3-TetramethylguanidineHCID 66460—
反応物2,2'-Anhydro-1-beta-arabinofuranosylthymineHCID 168045—
溶媒DimethylformamideHCID 6228—
生成物2'-Deoxy-2'-methylthio-5-methyluridineHCID 1033429374.1%

反応手順

2.2′-Anhydro-5-methyluridine (17.02 g, 70.6 mmol), methanethiol (16.3 g, 339 mmol), 1,1,3,3-tetramethylguanidine (40.6 g, 353 mmol), and dimethylformamide (150 ml) were heated together at 60° C. After 12 hr, the products were cooled and concentrated under reduced pressure. The residual oil was purified by short silica gel (300 g) column chromatography. Concentration of appropriate fractions, which were eluted with CH2Cl2-MeOH (93:7, v/v), furnished the title compound as a white foam (15.08 g, 74.1%). Crystallization from EtOH-CH2Cl2 furnished white needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06307040B1
出典データセットuspto-grants-2001_10
ORD IDord-6b367e86d8654ac4a8f7118bd2a4d660
出典メモuspto-grants-2001_10