Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 66710940 | HCID 66710940 | — |
| Product | HCID 66710941 | HCID 66710941 | 91% |
Reaction Steps
7-(5-Chloro-2-methoxy-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine 7-(5-Chloro-2-methoxy-phenyl)-2-methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazine (0.730 g, 0.00239 mol) was dissolved in Methylene chloride (20 mL, 0.4 mol) and the mixture was treated with m-Chloroperbenzoic acid (0.556 g, 0.00322 mol). The reaction was allowed to stir at room temperature until HPLC showed consumption of starting material. The reaction was partitioned between sodium thiosulfate and DCM and the combined organic layers were dried over saturated sodium sulfate. The solution was filtered and reduced. The solid was then triturated with ether to afford 700 mg of 7-(5-Chloro-2-methoxy-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine as a yellow powder. (M+H)=322.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-0f204b6e6dfd47809d790d85b292a4b8 |
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| Source note | uspto-grants-2013_06 |
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