Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Reactant | HCID 10035419 | HCID 10035419 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21915676 | HCID 21915676 | 86% |
Reaction Steps
A mixture of 1-methyl-2-carbamoyl-5-hydroxy-1H-indole (0.875 g; 4.6 mmol), 2-nitrobenzyl bromide (1 g; 4.63 mmol) and Cs2CO3 (1.5 g; 4.63 mmol) in acetonitrile (55 ml) was heated at 90° C. under argon atmosphere for 2 h 30. After evaporation to dryness, the residue was extracted with CH2Cl2/H2O. The organic phase was evaporated and the residue triturated in CH2Cl2/ether to give 1-methyl-2-carbamoyl-5-(3-nitrobenzyloxy)-1H-indole as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125906B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-08681d5529e14b7ca912f8655d8e5a00 |
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| Source note | uspto-grants-2006_10 |
|---|