HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67032868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 3,4-Dihydro-7-iodo-2(1H)-quinolinone | HCID 58851400 | — |
| Product | HCID 67032868 | HCID 67032868 | — |
Reaction Steps
According to the Step 8-1 in synthetic method for EXAMPLE aa8, 3,4-dihydro-7-iodo-2(1H)-quinolinone (2.12 g) and bromoacetic acid methyl ester (1.10 mL) were used instead of aa7-1 and MeI to obtain compound aa21-1 (2.24 g) as a white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987242B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-1a293eb2720644198dc007a49d9d0a66 |
| Source note | uspto-grants-2015_03 |