Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 67109260 | HCID 67109260 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 51347782 | HCID 51347782 | — |
Reaction Steps
2-(3,5-dimethylisoxazol-4-yl)-3-(4-methoxyphenyl)-1H-indole-1-carbonitrile was dissolved in 3 ml DCM and the mixture was cooled to −50° C. BBr3 (5 eq) was added and the reaction was stirred at −50° C. for 4.5 h and then at −20° C. for 16 h. The mixture was cooled to −78° C. and MeOH (90 μl) was added followed by water. The aqueous layer was extracted with DCM 3× and the combined organic layers were concentrated. The crude product was purified on silica (EtOAc/n-Heptane 2:8-3:7). 4.9 mg 2-(3,5-dimethylisoxazol-4-yl)-3-(4-hydroxyphenyl)-1H-indole-1-carbonitrile was obtained as a white solid. ES/MS m/z: 330.2 (M+H), 328.3 (M−H); 1H NMR (CDCl3, 500 MHz): 7.75 (m, 1H), 7.67 (m, 1H), 7.51 (m, 1H), 7.41 (m, 1H), 7.20 (m, 2H), 6.88 (m, 2H), 2.28 (s, 3H) and 2.05 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710243B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-830bec240bf34dd18c0e363c17005d42 |
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| Source note | uspto-grants-2014_04 |
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