HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406174Generated: October 30, 2026
1,3-Dimethyl-2-imidazolidinone → HCID 66665632, compound
https://huagongshe.com/reaction/406174
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 86681846 | HCID 86681846 | — |
| Reactant | HCID 178471412 | HCID 178471412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66665632 | HCID 66665632 | — |
Reaction Steps
A mixture comprising lithium bromide (307 mg, 3.54 mmol) and PEPPSi-iPr catalyst (75 mg, 0.110 mmol) in THF (2 ml) was stirred at room temperature for 15 minutes until a solution formed. (6-Ethoxy-6-oxohexyl)zinc(II) bromide (13.26 ml of a 0.5M solution in THF, 6.62 mmol) was added and the mixture was cooled to 0° C. A solution of 7-chloro-2,3-diphenyl-1,8-naphthyridine (step 1) (350 mg, 1.105 mmol) in THF (3 ml)/DMI (1 ml) was added and the resulting mixture was stirred at room temperature for 24 h. The reaction mixture was partitioned between EtOAc and water and the organic portion was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude product by chromatography on silica eluting with 0-50% EtOAc in iso-hexane afforded the title product as a yellow oil; LC-MS Rt=1.54 mins; [M+H]+425.3, Method 2minLC_v002
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754085B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-933372fc2c32482e8f3bcaefdd54857b |
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| Source note | uspto-grants-2014_06 |
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