HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67034282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | 3,4-Dihydro-7-iodo-2(1H)-quinolinone | HCID 58851400 | — |
| Product | HCID 67034282 | HCID 67034282 | — |
Reaction Steps
According to the Step 8-1 in synthetic method for EXAMPLE aa8, 3,4-dihydro-7-iodo-2(1H)-quinolinone (1.50 g) and cyclopropylmethyl bromide (0.80 mL) were used instead of a7-1 and MeI to obtain compound aa20-1 (1.23 g) as a pale red amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987242B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-572407efabd940bcbf99af7ff6b8fafb |
| Source note | uspto-grants-2015_03 |