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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218585Generated: October 31, 2026

Dimethylformamide → [4-N-(Piperonyloxycarbonyl)-cytosin-1-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/2218585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPiperonyl alcoholHCID 10322—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 21868458HCID 21868458—
Product[4-N-(Piperonyloxycarbonyl)-cytosin-1-yl]-acetic acid ethyl esterHCID 6852423196%

Reaction Conditions

Temperature100 °C

Reaction Steps

The reaction mixture of (cytosin-1-yl)-acetic acid (3.94 g, 20 mmol) and 1,1′-carbonyldiimidazole (4.86 g, 30 mmol) in DMF was stirred for 25 min. at 100° C. Then, piperonyl alcohol (6.08 g, 40 mmol) was added to the reaction mixture. The resulting reaction mixture was allowed to cool to room temperature for 2 h. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate (100 mL). The solution was washed with water (100 mL×2), dried over MgSO4, and filtered. The filtrate was concentrated in vacuo and treated with ethyl ether to afford white solid. The solid was filtered off and dried in vacuo to give the desired product (7.20 g, 96%). 1H-NMR (500 MHz; DMSO-d6) δ 10.77 (s, 1H), 8.04 (d, 1H), 7.04 (d, 1H), 7.00 (s, 1H), 6.92 (s, 2H), 6.02 (s, 2H), 5.09 (s, 2H), 4.61 (s, 2H), 4.15 (q, 2H), 1.19 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411065B2
Source datasetuspto-grants-2008_08
ORD IDord-bc399312917747c8b62cbb4b0c3c531e
Source noteuspto-grants-2008_08