Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | HCID 58203502 | HCID 58203502 | — |
| Product | HCID 58203527 | HCID 58203527 | 65% |
Reaction Steps
AcBr (3 mL) was added to 6-methyl-1-(5-isopropyl-2,6-dimethoxy-pyrimidin-4-yl)-1H-indole-4-carbonitrile (470 mg, 1.40 mmol). The reaction mixture was heated at 70° C. for 6 hours. The reaction mixture was then cooled to room temperature and concentrated. The crude reaction product was purified (silica gel, 0-80% EtOAc/hexane) to give a white solid (280 mg, 65%). LC-MS shows 307.1 (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-91b4b5ca05e1467e81ea0b6df9e6c140 |
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| Source note | uspto-grants-2012_12 |
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