HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906641Generated: October 29, 2026
Dimethylbarbituric acid → HCID 67401263, compound
https://huagongshe.com/reaction/906641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | m-Anisoyl chloride | HCID 74374 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67401054 | HCID 67401054 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67401263 | HCID 67401263 | 37% |
Reaction Steps
A solution of 326a (134 mg, 0.3 mmol), 1,3 Dimethylbarbituric acid (94 mg, 0.6 mmol) and Tetrakis(triphenylphosphine)palladium (12 mg, 0.01 mmol) were stirred under Argon in 3 mL CH2Cl2. The reaction was followed by HPLC until all starting material disappeared. The crude was evaporated to dryness and taken up in dry THF. To this solution was added DIEA (230 ul, 1.5 mmol) and 3-anisoylchloride 0.3 mmol). The reaction was stirred for 3 h, EtOAc was added and the organic layer was extracted with NaHCO3 sat, HCl (0.1N) and brine. The dry solution was evaporated and purified by flash chromatography on silica gel using cyclohexane/EtOAc 7:3 as eluent. 326 was obtained as an oil (54 mg, 37%): H1 NMR (CDCl3) δ 7.43-7.25 (m, 4H), 7.15-7.05 (m, 2H), 6.60 (m, 1H), 4.83 (d, J=6.0 Hz, 2H), 3.86 (s, 3H), 3.35 (d, J=6.6, 2H), 335-3.23 (m, 3H), 2.95 (m, 2H), 1.94 (m, 2H), 1.86 (m, 2H), 1.70-1.50 (m, 5H), 1.30-1.20 (m, 8H), 0.87 (t, J=6.8, 3H), M/Z APCI: 495.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012995B1 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-619504d190014e88b882fa3e5b8944a8 |
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| Source note | uspto-grants-2011_09 |
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