HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 66970088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | AX-9657 | HCID 25205741 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66970088 | HCID 66970088 | 156.1% |
Reaction Steps
To a solution of compound 132 (30 mg, 0.076 mmol) in dichloromethane (380 μL) was added methyl iodide (14.2 μL, 0.228 mmol) and the resulting mixture was stirred at ambient temperature for 2 hours. The solution was concentrated, and the residue was purified using preparative HPLC. The fractions containing the desired compound were lyophilized to yield compound 232 (27.8 mg, 89%) as a yellow powder. 1H NMR (CDCl3, 400 MHz) δ: 8.30 (dd, 1H, J=4.5 Hz), 8.11 (dd, 1H, J=1.6 Hz), 6.95 (d, 1H, J=2.4 Hz), 6.89 (m, 2H), 4.74 (m, 1H), 4.13 (m, 1H), 3.94 (s, 3H), 3.91 (m, 1H), 3.52 (m, 2H), 3.43 (s, 9H), 3.19 (m, 2H), 2.52 (m, 1H), 2.33 (m, 1H), 1.92 (s, 3H), 1.29 (t, 3H, J=7.5 Hz). ESMS m/z: 409.1 [M+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879846B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-8676345a3eda4499827f87109f5e64aa |
| Source note | uspto-grants-2011_02 |