HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 54476646, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 53797197 | HCID 53797197 | — |
| Product | HCID 54476646 | HCID 54476646 | — |
Reaction Steps
This compound was then converted to N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl]cyclobutanecarboxamide, mp 155°-157° C., by the procedure of Example 1 and further alkylated by the procedure of Example 6, using methyl iodide to give 8.32 g of N-[3-[3-(dimethylamino)1-oxo-2-propenyl]phenyl]-N-methylcyclobutanecarboxamide, mp 117°-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04626538 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-258971c8e443418aacebcdc3ef45828a |
| Source note | uspto-grants-1986_12 |