HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Amino-1,3-dihydropyrrol[4,3,2-de]isoquinoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-Ethoxy-1,3-dihydropyrrolo[4,3,2-de]isoquinoline | HCID 21515522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-1,3-dihydropyrrol[4,3,2-de]isoquinoline hydrochloride | HCID 21515520 | — |
| Product | 5-Amino-1,3-dihydropyrrolo[4,3,2-de]isoquinoline | HCID 21515521 | — |
Reaction Steps
To a suspension of 5-ethoxy-1,3-dihydropyrrolo[4,3,2-de]isoquinoline (200 mg, 1 mmole), described in Example 5, in ethanol (2 ml), aqueous ammonium hydroxide (25%, 0.5 ml, 1.4 mmole) is added followed by 2.3 N HCl in ethanol (0.5 ml). The mixture is heated at reflux for 0.5 hour, then ether is added and the light green crystalline precipitate collected to give the hydrochloride salt of the title compound, 5-amino-1,3-dihydropyrrol[4,3,2-de]isoquinoline hydrochloride, mp 227° - 228°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978066 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-62f82ea11cf54520bb531ed43a5f9e8e |
| Source note | uspto-grants-1976_08 |