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HRID 84065作成日:2026年10月26日

Ammonia → N4-(3,5,5-trimethyl-1-hexanoyl)-2'-deoxycytidine

https://huagongshe.com/reaction/84065

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物ChlorotrimethylsilaneHCID 6397—
反応物DeoxycytidineHCID 13711—
反応物3,5,5-Trimethylhexanoyl chlorideHCID 161929—
溶媒PyridineHCID 1049—
生成物N4-(3,5,5-trimethyl-1-hexanoyl)-2'-deoxycytidineHCID 86698897127.9%

反応手順

Suspending 2′-Deoxycytidine (2.3 g, 10.0 mmol) in dry pyridine, followed by concentration under reduced pressure was repeated 3 times to perform dehydrative azeotropic distillation, the concentrate was suspended again in dry pyridine (60 ml), and trimethylsilyl chloride (6.4 ml, 50 mmol) was added dropwise over 5 min. To the reaction mixture was added 3,5,5-trimethyl-1-hexanoyl chloride (9.5 ml, 50.0 mmol) over 5 min. After completion of the reaction, under ice-cooling, aqueous ammonia (25 ml) was added and the mixture was reacted for 20 min. The reaction mixture was concentrated under reduced pressure. Water (150 ml) was added to the concentrate, and the mixture was extracted 3 times with ethyl acetate (100 ml). The organic layer was concentrated and the obtained oil was purified by silica gel column chromatography to give the title compound (4.7 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846885B2
出典データセットuspto-grants-2014_09
ORD IDord-e1342269c6c64ced828ebd7673f082dc
出典メモuspto-grants-2014_09