HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzimidazole → N1-(1H-benzo[d]imidazol-2-yl)propane-1,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzimidazole | HCID 13624 | — |
| Reactant | HCID 86591654 | HCID 86591654 | — |
| Product | N1-(1H-benzo[d]imidazol-2-yl)propane-1,3-diamine | HCID 11593576 | — |
Reaction Steps
3-{[(2-aminoanilino)carbothioyl]amino}propylcarbamate (ESI-MS; [M+H+]: 325.15), which was then converted with HgO/cat. S into the corresponding aminobenzimidazole (6.4 g; ESI-MS; [M+H+]: 291.15). After removal of the Boc group using TFA, the crude product obtained was boiled in CH3OH with addition of active carbon, filtered, evaporated and crystallized from CH3OH/methyl t-butyl ether; 6 g of beige solid; ESI-MS; [M+H+]: 191.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279468B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-cd404ac8509147f1a400930802b4ae79 |
| Source note | uspto-grants-2007_10 |