HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-3-Bromopropylphthalimide → 2-(3-(4-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Reactant | 2-Ethylimidazole | HCID 66130 | — |
| Reactant | HCID 178418800 | HCID 178418800 | — |
| Product | 2-(3-(4-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione | HCID 13618120 | — |
| Product | 2-[3-(2-ethyl-1H-imidazol-1-yl)-propyl]isoindole-1,3(2H)-dione | HCID 13618121 | — |
Reaction Steps
Following the procedure of this example, N-(3-bromopropyl)phthalimide with 4-methylimidazole and 2-ethylimidazole were used to produce respectively 2-[3-(4-methyl-1H-imidazol-1-yl)propyl]isoindole-1,3-(2H)-dione and 2-[3-(2-ethyl-1H-imidazol-1-yl)-propyl]isoindole-1,3(2H)-dione which again following the procedure of this example were converted respectively to (4-methyl-1H-imidazol-1-yl)-1-propanamine dihydrochloride and (2-ethyl-1H-imidazol-1-yl)-1-propanamine dihydrochloride which were then converted by the procedure of Example 1, using the appropriate acid chloride, to the products of Examples 21-27, listed in Table V.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04489089 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-0a6365ca304746efbdac8c271989a1d4 |
| Source note | uspto-grants-1984_12 |