HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 1-{1-[2-(2-methoxynaphthalen-1-yl)ethyl]piperidin-4-yl}-1H-indole-6-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-(2-Methoxynaphthalen-1-yl)acetaldehyde | HCID 54479553 | — |
| Reactant | 1-(piperidin-4-yl)-1H-indole-6-carboxamide | HCID 57682786 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{1-[2-(2-methoxynaphthalen-1-yl)ethyl]piperidin-4-yl}-1H-indole-6-carboxamide | HCID 57682919 | 58.5% |
Reaction Steps
70 mg of 1-(piperidin-4-yl)-1H-indole-6-carboxamide and 115 mg of (2-methoxynaphthalen-1-yl)acetaldehyde were dissolved in 2 ml of tetrahydrofuran. Thereafter, 0.03 ml of acetic acid and 91 mg of sodium triacetoxyborohydride were added to the reaction solution, and the obtained mixture was then stirred at room temperature overnight. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction solution, and then extracted with chloroform. The extract was dried over magnesium sulfate and then concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-methanol), so as to obtain 72 mg of the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538123B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-a5a77a2a480c4f4184c10240c3b3ee18 |
| Source note | uspto-grants-2009_05 |