Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59508063 | HCID 59508063 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59508087 | HCID 59508087 | — |
Reaction Steps
A suspension of 2-(2-methoxypyridin-3-yl)-N-(3-morpholinopropyl)-1H-indole-5-carboxamide (0.850 g, 0.215 mmol) in 100 ml THF was heated to 60° C. until dissolved. To the solution was added N-bromosuccinimide (0.406 g, 0.263 mmol) and the reaction was allowed to stir for 1.5 hours. The reaction was not complete, so more N-bromosuccinimide (0.062 g, 0.35 mmol; 0.040 g, 0.022 mmol) was added sequentially and the reaction stirred for 10 more minutes after each addition. Upon completion, the reaction was concentrated and to the residue was added 50 ml EtOAC and 100 ml water. The organics were separated, washed with water (50 ml) and brine (25 ml) and concentrated. The crude product was used with no further purification. LCMS: 473 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410144B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-91889ed1093745c5b71c9786d3576afa |
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| Source note | uspto-grants-2013_04 |
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