HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606059Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 86616879, compound
https://huagongshe.com/reaction/606059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 21913508 | HCID 21913508 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86616879 | HCID 86616879 | — |
Reaction Steps
To dichloromethane (10 mL) at −78° C. was added dimethylsulfoxide (0.37 mL, 5.17 mmol) and oxalyl chloride (0.33 mL, 3.79 mmol). After several minutes, a solution of 2-[8-(ethoxymethyl)-5,6-dimethyl-7H-imidazo[4,5-c]tetraazolo[1,5-a]pyridin-7-yl]ethanol (prepared as described in U.S. Pat. No. 6,797,718, 1.00 g, 3.44 mmol) in dichloromethane (40 mL) was added dropwise followed by triethylamine (1.5 mL, 10.3 mmol). The mixture was allowed to warm to room temperature and more dichloromethane (80 mL) was added. The solution was transferred to a separatory funnel and washed with saturated aqueous potassium carbonate, water, and brine. The aqueous layers were combined and back-extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield the product [8-(ethoxymethyl)-5,6-dimethyl-7H-imidazo[4,5-c]tetraazolo[1,5-a]pyridin-7-yl]acetaldehyde as a tan solid (0.86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915281B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-2aa937961a14404e8a4e86f6f504c78c |
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| Source note | uspto-grants-2011_03 |
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