HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 136404509, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 136147901 | HCID 136147901 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 136404509 | HCID 136404509 | 67.6% |
Reaction Steps
Methyl iodide (200 mg) was added to a stirred solution of 1-methyl-4-[3-(methylindol-3-yl)-1,2,4-oxadiazol-5-yl]piperidine (300 mg) in anhydrous acetone (20 ml) at room temperature. After stirring at room temperature for two hours the precipitate was isolated by filtration and dried to afford the title compound (300 mg) mp 246° C.; Found C, 49.00; H, 5.30; N, 12.51 C18H23N4OI requires C, 49.32; H, 5.29; N, 12.78%; δH (360 MHz, DMSO) 2.25-2.35 (4 H, m, 2×CH2), 3.14 (3 H, s, NMe), 3.18 (3 H s NMe), 3.41 (1 H, m, CH), 3.48-3.56 (4 H, m, 2×CH2N), 3.90 (3 H, s, NMe), 7.22-7.33 (2 H, m, H-5, H-6), 7.58 (1 H, d, J=7, H-7), 8.05 (l H, d, J=7, H-4), 8.12 (1 H, s, H-2); M/Z (no M+), 199(90), 140(100), 96(90).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041456 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-2beeaa6f4aeb4c5d87fa9845a0634581 |
| Source note | uspto-grants-1991_08 |