Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 58203484 | HCID 58203484 | — |
| Product | HCID 67050506 | HCID 67050506 | 47.4% |
Reaction Steps
In a 10 mL round bottom flask, 1 mL AcBr was added to 3-(5-Isopropyl-2,6-dimethoxy-pyrimidin-4-yl)-quinoline (14 mg, 0.045 mmol). The reaction mixture was heated at 70° C. for 2 hours. The reaction mixture was concentrated down and purified by reverse phase prep HPLC (MeCN/water) to give a white powder (6 mg, 47%). LC-MS shows 280.3 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334295B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-cc645a165b1c4527b4b84ac082084824 |
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| Source note | uspto-grants-2012_12 |
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