HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 21964305, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Ethyl 5-Bromoindole-2-carboxylate | HCID 259091 | — |
| Product | HCID 21964305 | HCID 21964305 | — |
Reaction Steps
The title compound was prepared from ethyl 5-bromo-1H-indole-2-carboxylate and 4-methylbenzyl bromide in substantially the same manner, as described in Step 1 of Example 25. The product was obtained as a semi-solid contained 0.8 mole equivalent DMF. Mass spectrum (ESI, [M+H]+) m/z 372. 1H NMR (400 MHz, DMSO-d6) δ7.93 (d, 1H, J=7.94 Hz), 7.55 (d, 1H, J=9.01 Hz), 7.40 (dd, 1H, J=8.85 and 1.98 Hz), 7.32 (s, 1H), 7.04 (d, 2H, J=7.96 Hz), 6.90 (d, 2H, J=7.94 Hz), 5.79 (s, 2H), 4.28 (q, 2H), 2.20 (s, 3H), and 1.28 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368471B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-d10493aa1022447d9f946062aaac4ba2 |
| Source note | uspto-grants-2008_05 |