HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518788Generated: November 2, 2026
Hydrogen Peroxide → HCID 86697956, compound
https://huagongshe.com/reaction/518788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | HCID 86697957 | HCID 86697957 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86697956 | HCID 86697956 | 70.4% |
Reaction Steps
230 mg of methyl 7-(1-methyl-1H-pyrazol-4-yl)-2-(methylsulfanyl)thieno[3,2-d]pyrimidine-6-carboxylate, prepared by analogy with the method described in example 4, are added to a mixture of 25 equivalents of hydrogen peroxide (30% in water) and 1.49 g of phenol. The reaction medium is stirred for 30 minutes at ambient temperature and then heated at 50° C. for 1 hour. The reaction medium is diluted in ethyl acetate and washed with a saturated aqueous NaHCO3 solution and then with a saturated sodium chloride solution. The organic phase is dried over magnesium sulfate, filtered, and then concentrated under vacuum so as to obtain the crude product, which is purified on silica, elution being carried out with a 0-10% gradient of methanol in dichloromethane so as to obtain 170 mg of methyl 7-(1-methyl-1H-pyrazol-4-yl)-2-(methylsulfinyl)thieno[3,2-d]pyrimidine-6-carboxylate in the form of a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115140B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-6795a2571e8a4b66926e6954d0e1359a |
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| Source note | uspto-grants-2015_08 |
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