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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446038Generated: October 26, 2026

Pyridine → 2'-Deoxy-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}cytidine

https://huagongshe.com/reaction/1446038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDeoxycytidine hydrochlorideHCID 107488—
ReactantFluorenylmethyl chloroformateHCID 14261773—
Product2'-Deoxy-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}cytidineHCID 1430999697%

Reaction Steps

In one embodiment, 5′-O-DMTR-N4-FMOC-2′-deoxycytidine was prepared according to the following protocol. 30 g (37.9 mmol) of 2′-deoxycytidine hydrochloride were silylated with trimethylchlorosilane (75 ml) in pyridine (160 ml), followed by treatment with fluorenylmethoxycarbonyl chloride (33 g, 128 mmol). After hydrolysis with H2O (300 ml) and extraction with AcOEt/H2O, the N4-FMOC-2′-deoxycytidine was obtained in a 97% yield (49.5 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07667033B2
Source datasetuspto-grants-2010_02
ORD IDord-de5df47c417f476d9a3330a366acd292
Source noteuspto-grants-2010_02