Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66657350 | HCID 66657350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86600870 | HCID 86600870 | 80.7% |
Reaction Steps
59.7 mg (0.128 mmol) of (rac.) 5-{[6-fluoro-2-hydroxy-5-methoxy-4,4,7-trimethyl-2-(trifluoromethyl)-1,2,3,4-tetrahydronaphthalen-1-yl]amino}-isoquinolin-1(2H)-one is mixed at 0° C. with 1.3 ml of a 1 molar solution of boron tribromide in dichloromethane, and it is stirred for one hour at 0 to 5° C. At -10C, saturated sodium bicarbonate solution is now carefully added in drops. After 10 minutes of vigorous stirring at room temperature, the batch is extracted three times with methyl tert-butyl ether. The organic phases are dried, and after the solvent is spun off, the residue is chromatographed on a Flashmaster. 46.5 mg (80.3%) of the desired compound is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659297B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-98f628aa6a504d1792a8a235d17a95b8 |
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| Source note | uspto-grants-2010_02 |
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