HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(3-[(2-chloro-1-oxo-ethyl)methylamino]propyl)-10,11-dihydro-5H-dibenzo[b,f]azepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Desipramine | HCID 2995 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(3-[(2-chloro-1-oxo-ethyl)methylamino]propyl)-10,11-dihydro-5H-dibenzo[b,f]azepine | HCID 54151629 | — |
Reaction Steps
Dissolve 5-(3-methylaminopropyl)-10,11-dihydro-5H-dibenzo[b,f]azepine (7.0 g, 0.026 mol) and triethylamine (4 mL) in dichloromethane (100 mL) and cool with an ice-bath. Add, by dropwise addition, a solution of chloroacetyl chloride (3.23 g, 0.0286 mol) in dichloromethane (25 mL). Stir at room temperature for 12 hours, shake with dilute hydrochloric acid and dry (MgSO4). Evaporate the solvent in vacuo to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05182387 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-872fb14a53a543a7bdc4ab7d5d6600e5 |
| Source note | uspto-grants-1993_01 |