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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84065Generated: October 26, 2026

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

https://huagongshe.com/reaction/84065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDeoxycytidineHCID 13711—
Reactant3,5,5-Trimethylhexanoyl chlorideHCID 161929—
SolventPyridineHCID 1049—
ProductN4-(3,5,5-trimethyl-1-hexanoyl)-2'-deoxycytidineHCID 86698897127.9%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846885B2
Source datasetuspto-grants-2014_09
ORD IDord-e1342269c6c64ced828ebd7673f082dc
Source noteuspto-grants-2014_09