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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373050Generated: October 31, 2026

Cesium carbonate → 4-(4-Chloro-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl)-benzoic acid tert-butyl ester

https://huagongshe.com/reaction/1373050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantThymine, 6-chloro-HCID 3014023—
ReactantTert-butyl 4-(bromomethyl)benzoateHCID 11414578—
ReactantDichloromethane methanolHCID 21226129—
SolventDimethylformamideHCID 6228—
Product4-(4-Chloro-5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-ylmethyl)-benzoic acid tert-butyl esterHCID 6937400340.3%

Reaction Steps

5-Methyl-6-chloropyrimidine-2,4-dione (1.00 g, 6.22 mmol) was dissolved in dimethylformamide (15 mL).To the solution was added cesium carbonate (2.02 g, 6.22 mmol) and t-butyl 4-bromomethylbenzoate (1.69 g, 6.22 mmol). The mixture was stirred at room temperature for 20 hours. The solvent was evaporated under a vacuum at 60° C. The residue was mixed with tetrahydrofuran (50 mL) and methanol (10 mL) and filtered. The filtrate was evaporated in a vacuum to an amber oil. The oil was purified by flash chromatography on silica gel eluting first with dichloromethane then with dichloromethane:methanol (19:1) to give the desired product (0.88 g, 40% yield). 1H-NMR (DMSO-d6) δ 11.8 (s, 1H), 7.85 (d, 2H), 7.34 (d, 2H), 5.22 (s, 2H), 1.88 (s, 3H), 1.51 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160893B2
Source datasetuspto-grants-2007_01
ORD IDord-eb8dabc316a54c8b8f05a76b86cfb603
Source noteuspto-grants-2007_01