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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340785Generated: October 31, 2026

Dimethylbarbituric acid → HCID 53372245, compound

https://huagongshe.com/reaction/340785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylbarbituric acidHCID 69860—
ReactantHCID 67410049HCID 67410049—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 53372245HCID 53372245—

Reaction Steps

The title compound was prepared from ethyl 2-({[5-(biphenyl-4-yl)-6-chloro-1-(prop-2-en-1-yl)-1H-benzimidazol-2-yl]oxy}methyl)cyclopropanecarboxylate (115 mg, 0.236 mmol), 1,3-dimethylbarbituric acid (111 mg, 0.708 mmol), Pd(PPh3)4 (30 mg, 0.026 mmol) and EtOH (2.5 ml) according to the procedure described for Example 13, Step B. Purification of the resulting crude product by reverse phase HPLC eluting with 35-100% MeCN:water afforded the title compound as a white solid. LC-MS: calculated for C24H19ClN2O3 418.11, observed m/e: 418.97 (M+H)+ (Rt 2.12/4 min). 1H NMR (500 MHz, CD3OD): 7.75-7.35 (m, 11H), 4.50 (dd, 2H), 4.30 (dd, 2H) 1.85 (m, 1H), 1.70 (m, 1H), 1.10 (m, 11H), 1.05 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895596B2
Source datasetuspto-grants-2014_11
ORD IDord-1cdb52c1c19746d5892daeafd2ad3bf9
Source noteuspto-grants-2014_11