HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoquinoline → Ethyl 5-methyl-2-(quinolin-3-ylamino)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | Ethyl 2-amino-5-methylbenzoate | HCID 12327280 | — |
| Product | Ethyl 5-methyl-2-(quinolin-3-ylamino)benzoate | HCID 67393797 | — |
Reaction Steps
Obtained (0.845 g, 97% of yield) following the procedure described in Example 14 (step B) starting from ethyl 2-amino-5-methylbenzoate (0.395 g, 2.20 mmol) and 3-bromoquinoline (0.46 g, 2.20 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536165B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-2f718ea7627647bb870dbdeac52b9508 |
| Source note | uspto-grants-2013_09 |