HuagongsheHuagongshe Chemistry Print Report · For research reference only
Desipramine Hydrochloride → 10,11-Dihydro-N-methyl-N-(3-pyridyl)-carbonyl-5H-dibenz(b,f)azepine-5-propanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Desipramine Hydrochloride | HCID 65327 | — |
| Reactant | 3-Pyridinecarbonyl chloride, hydrochloride (1:1) | HCID 88438 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 10,11-Dihydro-N-methyl-N-(3-pyridyl)-carbonyl-5H-dibenz(b,f)azepine-5-propanamine | HCID 86744726 | 62% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
Freshly prepared nicotinoyl chloride hydrochloride (0.55 g, 0.003 mol) was suspended in methylene chloride (12 ml) cooled to 5° C. and sodium bicarbonate (0.053 g, 0.0063 mol) was added. After 5 minutes, desipramine hydrochloride (0.75 g, 0.0025 mol) was added and the mixture was stirred for 3 hours at 5° C. The sodium chloride was removed by filtration and the organic solution was extracted with aqueous sodium bicarbonate, dried over sodium sulfate, filtered through Celite™ and concentrated. Ethyl ether (5 ml) was added to the oily residue and white crystals formed. Yield 62% (0.58 g), m.p. 84°-86° C. The product has the formula: ##STR1532##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05525727 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-23f18292f9b14defab07d25d3b3b1b95 |
| Source note | uspto-grants-1996_06 |