HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097414Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 24944540, compound
https://huagongshe.com/reaction/1097414
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 25032807 | HCID 25032807 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24944540 | HCID 24944540 | 79% |
Reaction Steps
In CH2Cl2, dissolved was 7-[3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl]-2-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyrimidine (Compound 101) (3.3 g, 8.06 mmol), and m-chloroperoxybenzoic acid (3.0 g, 12.09 mmol) was slowly added thereto. The mixture was stirred at room temperature. To the reaction mixture, NaHCO3 (aq) was added, and the resultant mixture was extracted three times with CH2Cl2. The extract was washed twice with brine, dried over MgSO4, filtered, and evaporated under reduced pressure to remove solvent. The mixture was purified via silica gel column chromatography (CH2Cl2/MeOH, 50/1) to obtain 3-[7-{3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl}-[1,2,4]triazolo[1,5-a]pyri midine-2-yl]-pyridine-N-oxide (Compound 102) (2.7 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143262B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-81b401fb431d4385bcf5423543a7add2 |
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| Source note | uspto-grants-2012_03 |
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