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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647182Generated: October 31, 2026

Diisopropylethylamine → HCID 22854322, compound

https://huagongshe.com/reaction/1647182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxylamine, O-phenethyl-, hydrochlorideHCID 202939—
Reactant9-(2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)-2,6-dichloro-9H-purineHCID 11693064—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22854322HCID 2285432266%

Reaction Steps

9-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-2,6-dichloro-9H-purine (2.0 g, 3.2 mmol), O-(2-phenylethyl)hydroxylamine hydrochloride (0.70 g, 4.0 mmol) and diisopropylethylamine (0.95 g, 7.4 mmol) were dissolved in 1,4-dioxan (40 ml) and heated at reflux for 3 days. After cooling the reaction mixture was diluted with dichloromethane (50 ml) and washed with water (2×30 ml). The organic phase was dried (MgSO4). Flash chromatography on a silica gel column, eluting with heptane/ethyl acetate (1/1) gave the desired product as a foam (1.54 g, 66%), 1H NMR (DMSO-d6)γ 3.05 (2H, t, --OCH2 --), 4.19 (2H, t,--CH2Ph), 4.70 (1H, dd, H-5'a), 4.80 (1H, dd, H-5'b), 4.90 (1H, dd, H-4'), 5.22 (1H, t, H-3'), 6.39 (1H, t, H-2'), 6.59 (1H, d, H-1'), 8.51 (1H, s H-8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05430027
Source datasetuspto-grants-1995_07
ORD IDord-0c278747c58449bd933b7f0a4e943a87
Source noteuspto-grants-1995_07