Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86629110 | HCID 86629110 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57646773 | HCID 57646773 | — |
Reaction Steps
200 mg of 4-(3-Chloro-isoquinolin-6-yloxy)-piperidine-1-carboxylic acid tert-butyl ester (178) were dissolved in 5 ml of CH3CN and heated to 85° C. Then a mixture of 148 mg of N-bromosuccinimide and 9 mg of AlBN was added as solid and the resulting mixture was heated to reflux for 1 h. The solvent was removed in vacuo and the residue subjected to flash column chromatography. The yield of the isolated product was 41% LCMS: detected mass: 441.03, Rt=2.41 min (Method #1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722671B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-1367b694c6f24b2faf07950cecf65ace |
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| Source note | uspto-grants-2014_05 |
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