HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 13037312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl Beta-Carboline-3-Carboxylate | HCID 105078 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13037312 | HCID 13037312 | 98% |
Reaction Steps
Following a procedure in Chem. Bio. Chem, 2009, 10, 889-895, N-bromosuccinimide (37 mg, 0.208 mmol) was added to a solution of ethyl 9H-pyrido[3,4-b]indole-3-carboxylate (50 mg, 0.208 mmol) in acetic acid (1.5 ml) and stirred at room temperature. After 45 minutes the acetic acid was removed and the solid material was partitioned between EtOAc and NaHCO3. The organic layer was washed with water, brine, and dried over Na2SO4 to afford the desired compound in 98% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877797B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-96c4d26eddfb46068f2006ad4dd2ed2b |
| Source note | uspto-grants-2014_11 |