HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzyl bromide → HCID 12019294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | HCID 12595022 | HCID 12595022 | — |
| Product | HCID 12019294 | HCID 12019294 | — |
Reaction Steps
Methyl 4-(4-bromobenzylamino)-2-methylquinoline-3-carboxylate was synthesized by the same method as described for 1-(4-(4-bromobenzylamino-2-methylquinolin-3-yl)ethanone (Example 1, Intermediate 2c), starting from methyl 4-amino-2-methylquinoline-3-carboxylate and 4-bromobenzyl bromide. Melting point: 89° C.; MS(ES+): 385/387.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06339077B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-8ea91c19ffd74f7a9b5cbbc019b02944 |
| Source note | uspto-grants-2002_01 |