HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-nitroquinoline → 3-({2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-ylamino}-methyl)-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-nitroquinoline | HCID 319251 | — |
| Reactant | 5-Methyl-2-furylmethylamine | HCID 2724683 | — |
| Reactant | 3-Formylbenzene-1-sulfonamide | HCID 18461734 | — |
| Product | 3-({2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-ylamino}-methyl)-benzenesulfonamide | HCID 24987862 | — |
Reaction Steps
The title compound, MS: m/e=423.1 (M+H+), was prepared from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and 3-formylbenzenesulfonamide (CAS 1778-37-6) as described in example 26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825253B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-9442637a6e834b4fa707cf1f34b0dfc2 |
| Source note | uspto-grants-2010_11 |