HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747277Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 59749538, compound
https://huagongshe.com/reaction/747277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 59749535 | HCID 59749535 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 59749538 | HCID 59749538 | 74.1% |
Reaction Steps
A Swern-type reagent was formed in standard fashion: oxalyl chloride (9.15 mL as a 2M soln. in CH2Cl2) in CH2Cl2 (23 mL) was cooled to −78° C. and treated with a solution of DMSO (2.85 mL, 36.8 mmol) in CH2Cl2 (23 mL) for 30 m. To this solution was added 5-{-1[2-(4-methoxy-benzylsulfanyl)-4,5-dihydro-3H-imidazol-4-yl]-ethyl}-quinoline (Intermediate E5) (4.7 g, 12.4 mmol) in CH2Cl2 (30 mL) and stirring continued for 45 m at −78° C. Triethylamine (9 mL) was added at −78° C. and warmed to rt for 40 m. The reaction mixture was diluted with brine and CH2Cl2. The aqueous layer was extracted with ethyl acetate. The organic solution was dried over MgSO4, filtered and evaporated to dryness. Chromatography on SiO2 with 80 to 100% ethyl acetate:hexanes yielded 5-{1-[2-(4-methoxy-benzylsulfanyl)-3H-imidazol-4-yl]-ethyl}-quinoline (Intermediate E6) 3.45 g (74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396849B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-dd489c62a0f94ed1a5b213c78e5c4baf |
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| Source note | uspto-grants-2008_07 |
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