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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369316Generated: October 25, 2026

5-Aminopentan-1-ol → 2'-deoxy-N4-(5-hydroxypentyl)-5'-O-(4,4'-dimethoxytrityl)cytidine

https://huagongshe.com/reaction/1369316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminopentan-1-olHCID 75634—
ReactantTriazabicyclodeceneHCID 79873—
ReactantN-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidineHCID 2724490—
SolventIsopropanolHCID 3776—
Product2'-deoxy-N4-(5-hydroxypentyl)-5'-O-(4,4'-dimethoxytrityl)cytidineHCID 12112520—

Reaction Steps

A solution of 5-aminopentanol (10.0 g, 96.9 mmol) in 2-propanol (10 mL) was added to N4-benzoyl-2′-deoxy-5′-O-(4,4′-dimethoxytrityl)cytidine (2.61 g, 4.12 mmol) and stirred until the mixture was clear. 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD, 2.40 g, 17.2 mmol) was added and the reaction mixture was stirred at ambient temperature for 48 hours. The reaction mixture was evaporated to an oil under high vacuum via oil pump, dissolved in CHCl3 (100 mL), extracted with 0.1 molar aqueous NaOH (2×50 mL) and water (4×50 mL). The organic phase was dried with anhydrous Na2SO4, evaporated, and dissolved in CH2Cl2. The organic phase was evaporated to an oil and purified by silica gel column chromatography using 2:4:94 Et3N:MeOH:CH2Cl2 and 2.5:5:92.5 Et3N:MeOH:CH2Cl2; v/v/v as the eluent. The purification was repeated until a reasonably pure product was obtained. The removal of side product 2′-deoxy-5′-O-(4,4′-dimethoxytrityl)-cytidine was responsible for the necessary of additional purification. After purification 0.53 g (18%) of the title compound was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576752B1
Source datasetuspto-grants-2003_06
ORD IDord-2e5a7f28a39943258acfc97f49023a2e
Source noteuspto-grants-2003_06