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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227252Generated: October 30, 2026

Pyridine → HCID 136367326, compound

https://huagongshe.com/reaction/227252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 136367327HCID 136367327—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 136367326HCID 13636732658.5%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a stirred solution of compound 1-2 from step 1 (5.85 g, 16.0 mmol) in pyridine (80 mL) is added benzoyl chloride (13.49 g, 96 mmol) and DMAP (0.05 g, 0.4 mmol) at RT. The reaction mixture is heated to 55° C. and then cooled to RT and stirred for 72 h. The reaction mixture is poured into saturated NaHCO3 (400 mL) and ethyl acetate (250 mL) and stirred for 1.5 h. The reaction mixture is extracted with ethyl acetate (2×1 L) and the combined organic extracts are washed with cold HCl (0.1 N, 400 mL), saturated NaHCO3 (1×200 mL), water (2×200 mL), and brine (1×250 mL) and dried (MgSO4). After filtration, the filtrate is concentrated and the crude residue is purified on silica gel column by flash chromatography using ethyl acetate in hexanes (0 to 100%) to afford 6.35 g (58.5%) of 3,4-bis-benzoyloxy-2-benzoyloxymethyl-5-(4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-7-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester (1-3) as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560434B2
Source datasetuspto-grants-2009_07
ORD IDord-82c0df05b03945f897b598094ffa1bb0
Source noteuspto-grants-2009_07