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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857543Generated: October 30, 2026

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

https://huagongshe.com/reaction/857543

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 numberUS07145006B2
Source datasetuspto-grants-2006_12
ORD IDord-23d343ff69ab4a0f89e482a2ebd741f4
Source noteuspto-grants-2006_12