HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836301Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 178437191, compound
https://huagongshe.com/reaction/1836301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178436743 | HCID 178436743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178437191 | HCID 178437191 | 51% |
Reaction Steps
To oxalyl chloride (0.85 μl, 0.976 mmol) in 5 ml of anhydrous dichloromethane at −78° C., dimethylsulfoxide (0.14 ml, 1.95 mmol) was added over a five minute period. After stirring for 5 minutes at the same temperature, 4-[1-(4,5-Dihydro-1H-imidazol-4-yl)-ethyl]quinoline (0.200 g, 0.888 mmol) was added slowly and the reaction mixture was stirred for a further 20 minutes at −78°. Triethylamine (0.62 ml, 4.44 mmol) was added and the reaction mixture was stirred for 5 minutes at −78° C. and then 20 minutes at room temperature. The reaction mixture was concentrated under reduced pressure and partitioned between EtOAc (10 ml) and water (5 ml). The organic layer was dried over sodium sulfate, filtered, concentrated and column purified [EtOAc:MeOH:Methanol NH3 (1.0 M); 3.5:1:0.5) to give 0.100 g (51%) of the product as a syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777426B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-87c6db1acbaa41149df09a7efbd6d89c |
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| Source note | uspto-grants-2004_08 |
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