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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480156Generated: October 30, 2026

Water → HCID 67079134, compound

https://huagongshe.com/reaction/480156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 86591745HCID 86591745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67079134HCID 6707913488.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]octane-1-carbothioic acid amide (20 mg, 50 μmol) and KLCO3 (8.0 eq, 400 μmol) in THF (5 ml) was stirred vigorously for 5 min and ethyl bromopyruvate (29 mg, 150 μmol) was added neat via syringe. The resulting, pale yellow solution was stirred at rt for 1 h, cooled to 0° C. with the aid of an ice bath and treated sequentially with pyridine (8.0 eq, 400 μmol) and (F3CCO)2O (4.0 eq, 42 mg, 200 μmol). The resulting deep red solution was allowed to reach ambient temperature overnight. Following the addition of water (4 ml), the mixture was concentrated in vacuo and extracted with CH2Cl2 (2×10 ml). The combined organic phases were washed with 2 N HCl, dried (Na2SO4), filtered and concentrated in vacuo. The solution was purified by radial chromatography (1 mm plate) using 2-5% MeOH in CH2Cl2 as eluent to afford a white solid (22 mg, 88%). MS: 500 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649600B1
Source datasetuspto-grants-2003_11
ORD IDord-15407ffc33ff408c828eb97b1f809ab5
Source noteuspto-grants-2003_11