HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570764Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 89488421, compound
https://huagongshe.com/reaction/570764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 71547715 | HCID 71547715 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89488421 | HCID 89488421 | — |
Reaction Steps
To a solution of N-[3-[[2,6-dibromo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-methyl-carbamoyl]-2-methoxy-phenyl]-N-methyl-pyridine-4-carboxamide (Example G-17) (0.051 g, 0.073 mmole) in dichloromethane (0.44 ml) was added by small portions 3-chloroperbenzoic acid (purity 70%) (0.027 g, 0.11 mmole). After 2.5 hours stirring at 25° C., the yellow solution was quenched with aqueous sodium sulfite, diluted with dichloromethane and washed twice with saturated aqueous sodium bicarbonate, then with brine. The organic solution was dried over sodium sulfate. The product (Compound G18 of Table G) was isolated after removal of the solvent, as a white powder (melting range: 105-194° C.) showing, by LC-MS analysis (method 6 described hereunder) a retention time of 0.99 min and a M+H+ peak of 716.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023873B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-649c246f0e29467595ef3cad8f6deb7d |
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| Source note | uspto-grants-2015_05 |
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