HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 89995372, compound → N-cyclohexyl-6-hydroxy-4-methyl-1H-indole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 89995372 | HCID 89995372 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-cyclohexyl-6-hydroxy-4-methyl-1H-indole-2-carboxamide | HCID 89995412 | 106.4% |
Reaction Steps
To a solution of 6-(benzyloxy)-N-cyclohexyl-4-methyl-1H-indole-2-carboxamide (I-9A-a: 1.5 g, 4.14 mmol) in ethanol (30 mL) was added 10% Pd—C (300 mg) and the mixture placed in a Parr hydrogenator (50 psi) at room temperature for 6 h. The reaction mixture was filtered through celite pad and washed with ethanol (30 mL), concentrated under reduced pressure to afford 1.2 g (90%) of N-cyclohexyl-6-hydroxy-4-methyl-1H-indole-2-carboxamide (I-9A-b) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447039B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d5f9a767edbc4f40815495f349f13dd1 |
| Source note | uspto-grants-2016_09 |