HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693290Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 67280305, compound
https://huagongshe.com/reaction/1693290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86641323 | HCID 86641323 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67280305 | HCID 67280305 | 61% |
Reaction Steps
A mixture composed of di-tert-butyl {8-hydroxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]-2,7,8,9-tetrahydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-4-yl}imidodicarbonate of Example 32 (778 mg), dimethyl sulfoxide (10 mL) and acetic anhydride (1 mL) was stirred in a nitrogen atmosphere at room temperature for 12 hours. After confirming that the raw material disappeared, the reaction mixture was diluted with ethyl acetate and sequentially washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and filtered. Then, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate-hexane) to obtain the title compound (507 mg, 61%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158638B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1b6d335d2fc7443f831e866f8beb19f9 |
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| Source note | uspto-grants-2012_04 |
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